Canonical Allele Identifier: CA2706446057

Gene: GC

Linked Data

• dbSNP Id: rs2149290616

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741871_71741872insAAAG , CM000666.2:g.71741871_71741872insAAAG	GRCh38
NC_000004.11:g.72607588_72607589insAAAG , CM000666.1:g.72607588_72607589insAAAG	GRCh37
NC_000004.10:g.72826452_72826453insAAAG	NCBI36
NG_012837.2:g.68649_68650insCTTT
NG_012837.3:g.68649_68650insCTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*26-2_*26-1insCTTT MANE Select	ENSP00000273951.8:n.*26-2_*26-1insCTTT
ENST00000273951.12:c.*26-2_*26-1insCTTT	ENSP00000273951.8:n.*26-2_*26-1insCTTT
ENST00000503364.5:n.124-2_124-1insCTTT
ENST00000503472.5:n.1335-2_1335-1insCTTT
ENST00000504199.5:c.*26-2_*26-1insCTTT	ENSP00000421725.1:n.*26-2_*26-1insCTTT
ENST00000509740.5:c.*274-2_*274-1insCTTT	ENSP00000422664.1:n.*274-2_*274-1insCTTT
ENST00000513476.5:c.1396-2_1396-1insCTTT	ENSP00000426683.1:n.1396-2_1396-1insCTTT
NM_000583.3:c.*26-2_*26-1insCTTT	NP_000574.2:n.*26-2_*26-1insCTTT
NM_001204306.1:c.*26-2_*26-1insCTTT	NP_001191235.1:n.*26-2_*26-1insCTTT
NM_001204307.1:c.*26-2_*26-1insCTTT	NP_001191236.1:n.*26-2_*26-1insCTTT
XM_006714177.2:c.*40-2_*40-1insCTTT	XP_006714240.1:n.*40-2_*40-1insCTTT
XM_006714177.3:c.*40-2_*40-1insCTTT	XP_006714240.1:n.*40-2_*40-1insCTTT
NM_000583.4:c.*26-2_*26-1insCTTT MANE Select	NP_000574.2:n.*26-2_*26-1insCTTT