Canonical Allele Identifier: CA14135874
Gene: NRG4 HGNC NCBI

Linked Data

dbSNP Id: rs11072566

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.76001630A>G , CM000677.2:g.76001630A>G GRCh38
NC_000015.9:g.76293971A>G , CM000677.1:g.76293971A>G GRCh37
NC_000015.8:g.74081026A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000394907.8:c.104+7570T>C MANE Select ENSP00000378367.3:n.104+7570T>C
ENST00000394907.7:c.104+7570T>C ENSP00000378367.3:n.104+7570T>C
ENST00000461391.5:c.104+7570T>C ENSP00000431810.1:n.104+7570T>C
ENST00000472094.5:c.104+7570T>C ENSP00000432751.1:n.104+7570T>C
ENST00000498750.5:c.104+7570T>C ENSP00000436832.1:n.104+7570T>C
ENST00000562114.5:c.104+7570T>C ENSP00000454895.1:n.104+7570T>C
ENST00000563204.5:c.104+7570T>C ENSP00000455314.1:n.104+7570T>C
ENST00000563910.5:c.104+7570T>C ENSP00000455167.1:n.104+7570T>C
ENST00000565661.5:c.104+7570T>C ENSP00000457838.1:n.104+7570T>C
ENST00000566417.5:c.104+7570T>C ENSP00000457335.1:n.104+7570T>C
ENST00000567126.5:c.104+7570T>C ENSP00000457626.1:n.104+7570T>C
ENST00000567936.5:c.104+7570T>C ENSP00000456029.1:n.104+7570T>C
ENST00000568073.5:c.104+7570T>C ENSP00000456778.1:n.104+7570T>C
NM_138573.3:c.104+7570T>C NP_612640.1:n.104+7570T>C
XM_017021937.2:c.104+7570T>C XP_016877426.1:n.104+7570T>C
XM_017021938.2:c.104+7570T>C XP_016877427.1:n.104+7570T>C
XM_017021939.2:c.104+7570T>C XP_016877428.1:n.104+7570T>C
XM_017021940.2:c.104+7570T>C XP_016877429.1:n.104+7570T>C
XM_017021941.2:c.104+7570T>C XP_016877430.1:n.104+7570T>C
XM_017021942.2:c.104+7570T>C XP_016877431.1:n.104+7570T>C
XM_017021943.2:c.104+7570T>C XP_016877432.1:n.104+7570T>C
XM_017021944.2:c.104+7570T>C XP_016877433.1:n.104+7570T>C
XM_017021945.2:c.104+7570T>C XP_016877434.1:n.104+7570T>C
XM_017021946.2:c.104+7570T>C XP_016877435.1:n.104+7570T>C
XM_017021947.2:c.104+7570T>C XP_016877436.1:n.104+7570T>C
XM_017021948.2:c.104+7570T>C XP_016877437.1:n.104+7570T>C
XM_024449847.1:c.104+7570T>C XP_024305615.1:n.104+7570T>C
XM_024449848.1:c.104+7570T>C XP_024305616.1:n.104+7570T>C
NM_138573.4:c.104+7570T>C MANE Select NP_612640.1:n.104+7570T>C