Canonical Allele Identifier: CA1467373957

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71758473_71758474delinsCA , CM000666.2:g.71758473_71758474delinsCA	GRCh38
NC_000004.11:g.72624190_72624191delinsCA , CM000666.1:g.72624190_72624191delinsCA	GRCh37
NC_000004.10:g.72843054_72843055delinsCA	NCBI36
NG_012837.2:g.52047_52048delinsTG
NG_012837.3:g.52047_52048delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.702-303_702-302delinsTG MANE Select	ENSP00000273951.8:n.702-303_702-302delinsTG
ENST00000273951.12:c.702-303_702-302delinsTG	ENSP00000273951.8:n.702-303_702-302delinsTG
ENST00000503472.5:n.586-303_586-302delinsTG
ENST00000504199.5:c.759-303_759-302delinsTG	ENSP00000421725.1:n.759-303_759-302delinsTG
ENST00000509740.5:c.702-303_702-302delinsTG	ENSP00000422664.1:n.702-303_702-302delinsTG
ENST00000513476.5:c.702-303_702-302delinsTG	ENSP00000426683.1:n.702-303_702-302delinsTG
NM_000583.3:c.702-303_702-302delinsTG	NP_000574.2:n.702-303_702-302delinsTG
NM_001204306.1:c.702-303_702-302delinsTG	NP_001191235.1:n.702-303_702-302delinsTG
NM_001204307.1:c.759-303_759-302delinsTG	NP_001191236.1:n.759-303_759-302delinsTG
XM_006714177.2:c.702-303_702-302delinsTG	XP_006714240.1:n.702-303_702-302delinsTG
XM_006714177.3:c.702-303_702-302delinsTG	XP_006714240.1:n.702-303_702-302delinsTG
NM_000583.4:c.702-303_702-302delinsTG MANE Select	NP_000574.2:n.702-303_702-302delinsTG