Canonical Allele Identifier: CA15541404
Gene: NRG1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10503887

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31775931G>T , CM000670.2:g.31775931G>T GRCh38
NC_000008.10:g.31633447G>T , CM000670.1:g.31633447G>T GRCh37
NC_000008.9:g.31752989G>T NCBI36
NG_012005.1:g.141180G>T
NG_012005.2:g.141710G>T

Transcript Alleles

HGVS Amino-acid change
NM_001159995.1:c.37+136500G>T VV NP_001153467.1:p.=
NM_001159999.1:c.37+136500G>T VV NP_001153471.1:p.=
NM_001160001.1:c.37+136500G>T VV NP_001153473.1:p.=
NM_013962.2:c.745+135202G>T VV NP_039256.2:p.=
XM_011544512.1:c.121+135202G>T XP_011542814.1:p.=
NM_001159995.2:c.37+136500G>T VV NP_001153467.1:p.=
NM_001159999.2:c.37+136500G>T VV NP_001153471.1:p.=
NM_001160001.2:c.37+136500G>T VV NP_001153473.1:p.=
NM_001322201.1:c.-556+136500G>T VV NP_001309130.1:p.=
NM_001322202.1:c.-505+136500G>T VV NP_001309131.1:p.=
XM_011544512.2:c.121+135202G>T XP_011542814.1:p.=
XM_017013365.2:c.121+135202G>T XP_016868854.1:p.=
XM_017013366.2:c.121+135202G>T XP_016868855.1:p.=
XM_017013367.1:c.121+135202G>T XP_016868856.1:p.=
XM_017013371.2:c.121+135202G>T XP_016868860.1:p.=
XM_017013372.2:c.121+135202G>T XP_016868861.1:p.=
ENST00000518104.5:c.37+136500G>T ENSP00000430053.1:p.=
ENST00000519301.5:c.37+136500G>T ENSP00000429582.1:p.=
ENST00000520407.5:c.745+135202G>T ENSP00000434640.1:p.=
ENST00000523534.5:n.304+135202G>T ENSP00000429067.1:p.=