Canonical Allele Identifier: CA2762138124

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741873_71741874del , CM000666.2:g.71741873_71741874del	GRCh38
NC_000004.11:g.72607590_72607591del , CM000666.1:g.72607590_72607591del	GRCh37
NC_000004.10:g.72826454_72826455del	NCBI36
NG_012837.2:g.68648_68649del
NG_012837.3:g.68648_68649del

Transcript Alleles

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