Canonical Allele Identifier: CA225659
Gene: NRG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 98395
ClinVar RCV Id: RCV000084686
dbSNP Id: rs367543164
gnomAD v3: 8-32756456-G-A
gnomAD v4: 8-32756456-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.32756456G>A , CM000670.2:g.32756456G>A GRCh38
NC_000008.10:g.32613974G>A , CM000670.1:g.32613974G>A GRCh37
NC_000008.9:g.32733516G>A NCBI36
NG_012005.1:g.1121707G>A
NG_012005.2:g.1122235G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405005.8:c.857G>A MANE Select ENSP00000384620.2:p.Arg286Gln
ENST00000522402.6:c.395G>A ENSP00000430862.2:p.Arg132Gln
ENST00000651333.2:c.1037G>A ENSP00000498590.1:p.Arg346Gln
ENST00000519301.6:c.707G>A ENSP00000429582.1:p.Arg236Gln
ENST00000650819.1:c.1037G>A ENSP00000498946.1:p.Arg346Gln
ENST00000650856.1:c.*30G>A ENSP00000498216.1:n.*30G>A
ENST00000650866.1:c.809G>A ENSP00000499045.1:p.Arg270Gln
ENST00000650980.1:c.848G>A ENSP00000498583.1:p.Arg283Gln
ENST00000651333.1:c.1037G>A ENSP00000498590.1:p.Arg346Gln
ENST00000651335.1:c.604+1982G>A
ENST00000651696.1:c.723G>A
ENST00000652588.1:c.971G>A ENSP00000498367.1:p.Arg324Gln
ENST00000652592.1:c.1037G>A ENSP00000498646.1:p.Arg346Gln
ENST00000652698.1:c.758G>A ENSP00000499008.1:p.Arg253Gln
ENST00000287842.7:c.872G>A ENSP00000287842.4:p.Arg291Gln
ENST00000356819.7:c.848G>A ENSP00000349275.6:p.Arg283Gln
ENST00000405005.7:c.857G>A ENSP00000384620.2:p.Arg286Gln
ENST00000518104.5:c.758G>A ENSP00000430053.1:p.Arg253Gln
ENST00000519240.5:c.386G>A ENSP00000428411.1:p.Arg129Gln
ENST00000519301.5:c.707G>A ENSP00000429582.1:p.Arg236Gln
ENST00000521670.5:c.857G>A ENSP00000428828.1:p.Arg286Gln
ENST00000522569.1:n.587G>A
ENST00000523079.5:c.848G>A ENSP00000430120.1:p.Arg283Gln
ENST00000523534.5:c.1076G>A ENSP00000429067.1:p.Arg359Gln
ENST00000539990.3:c.395G>A ENSP00000439276.2:p.Arg132Gln
NM_001159995.1:c.758G>A NP_001153467.1:p.Arg253Gln
NM_001159996.1:c.395G>A NP_001153468.1:p.Arg132Gln
NM_001159999.1:c.809G>A NP_001153471.1:p.Arg270Gln
NM_001160001.1:c.707G>A NP_001153473.1:p.Arg236Gln
NM_001160004.1:c.848G>A NP_001153476.1:p.Arg283Gln
NM_001160008.1:c.848G>A NP_001153480.1:p.Arg283Gln
NM_013956.3:c.872G>A NP_039250.2:p.Arg291Gln
NM_013957.3:c.848G>A NP_039251.2:p.Arg283Gln
NM_013960.3:c.857G>A NP_039254.1:p.Arg286Gln
NM_013964.3:c.857G>A NP_039258.1:p.Arg286Gln
XM_005273485.2:c.1037G>A XP_005273542.1:p.Arg346Gln
XM_005273486.2:c.1022G>A XP_005273543.1:p.Arg341Gln
XM_005273487.2:c.1013G>A XP_005273544.1:p.Arg338Gln
XM_006716335.2:c.197G>A XP_006716398.1:p.Arg66Gln
XM_011544512.1:c.893G>A XP_011542814.1:p.Arg298Gln
XM_011544513.1:c.1037G>A XP_011542815.1:p.Arg346Gln
XM_011544514.1:c.1022G>A XP_011542816.1:p.Arg341Gln
NM_001159995.2:c.758G>A NP_001153467.1:p.Arg253Gln
NM_001159996.2:c.395G>A NP_001153468.1:p.Arg132Gln
NM_001159999.2:c.809G>A NP_001153471.1:p.Arg270Gln
NM_001160001.2:c.707G>A NP_001153473.1:p.Arg236Gln
NM_001160004.2:c.848G>A NP_001153476.1:p.Arg283Gln
NM_001322197.1:c.386G>A NP_001309126.1:p.Arg129Gln
NM_001322201.1:c.83G>A NP_001309130.1:p.Arg28Gln
NM_001322202.1:c.83G>A NP_001309131.1:p.Arg28Gln
NM_001322205.1:c.1037G>A NP_001309134.1:p.Arg346Gln
NM_001322206.1:c.1037G>A NP_001309135.1:p.Arg346Gln
NM_001322207.1:c.1037G>A NP_001309136.1:p.Arg346Gln
NM_013956.4:c.872G>A NP_039250.2:p.Arg291Gln
NM_013957.4:c.848G>A NP_039251.2:p.Arg283Gln
NM_013960.4:c.857G>A NP_039254.1:p.Arg286Gln
NM_013964.4:c.857G>A NP_039258.1:p.Arg286Gln
XM_005273486.3:c.1022G>A XP_005273543.1:p.Arg341Gln
XM_005273487.3:c.1013G>A XP_005273544.1:p.Arg338Gln
XM_006716335.3:c.197G>A XP_006716398.1:p.Arg66Gln
XM_011544512.2:c.893G>A XP_011542814.1:p.Arg298Gln
XM_017013365.2:c.878G>A XP_016868854.1:p.Arg293Gln
XM_017013366.2:c.869G>A XP_016868855.1:p.Arg290Gln
XM_017013367.1:c.791G>A XP_016868856.1:p.Arg264Gln
XM_017013368.2:c.770G>A XP_016868857.1:p.Arg257Gln
XM_017013369.2:c.410G>A XP_016868858.1:p.Arg137Gln
XM_017013370.1:c.395G>A XP_016868859.1:p.Arg132Gln
XM_017013371.2:c.878G>A XP_016868860.1:p.Arg293Gln
XM_017013372.2:c.869G>A XP_016868861.1:p.Arg290Gln
XM_024447143.1:c.755G>A XP_024302911.1:p.Arg252Gln
NM_001159995.3:c.758G>A NP_001153467.1:p.Arg253Gln
NM_001159999.3:c.809G>A NP_001153471.1:p.Arg270Gln
NM_001160001.3:c.707G>A NP_001153473.1:p.Arg236Gln
NM_001160004.3:c.848G>A NP_001153476.1:p.Arg283Gln
NM_001160008.2:c.848G>A NP_001153480.1:p.Arg283Gln
NM_001322197.2:c.386G>A NP_001309126.1:p.Arg129Gln
NM_001322201.2:c.83G>A NP_001309130.1:p.Arg28Gln
NM_001322202.2:c.83G>A NP_001309131.1:p.Arg28Gln
NM_001322205.2:c.1037G>A NP_001309134.1:p.Arg346Gln
NM_001322206.2:c.1037G>A NP_001309135.1:p.Arg346Gln
NM_001322207.2:c.1037G>A NP_001309136.1:p.Arg346Gln
NM_013956.5:c.872G>A NP_039250.2:p.Arg291Gln
NM_013957.5:c.848G>A NP_039251.2:p.Arg283Gln
NM_013960.5:c.857G>A NP_039254.1:p.Arg286Gln
NM_013964.5:c.857G>A MANE Select NP_039258.1:p.Arg286Gln
NM_001159996.3:c.395G>A NP_001153468.1:p.Arg132Gln