Canonical Allele Identifier: CA2762138138

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741981_71741982insCA , CM000666.2:g.71741981_71741982insCA	GRCh38
NC_000004.11:g.72607698_72607699insCA , CM000666.1:g.72607698_72607699insCA	GRCh37
NC_000004.10:g.72826562_72826563insCA	NCBI36
NG_012837.2:g.68539_68540insTG
NG_012837.3:g.68539_68540insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*26-112_*26-111insTG MANE Select	ENSP00000273951.8:n.*26-112_*26-111insTG
ENST00000273951.12:c.*26-112_*26-111insTG	ENSP00000273951.8:n.*26-112_*26-111insTG
ENST00000503364.5:n.124-112_124-111insTG
ENST00000503472.5:n.1335-112_1335-111insTG
ENST00000504199.5:c.*26-112_*26-111insTG	ENSP00000421725.1:n.*26-112_*26-111insTG
ENST00000509740.5:c.*274-112_*274-111insTG	ENSP00000422664.1:n.*274-112_*274-111insTG
ENST00000513476.5:c.1396-112_1396-111insTG	ENSP00000426683.1:n.1396-112_1396-111insTG
NM_000583.3:c.*26-112_*26-111insTG	NP_000574.2:n.*26-112_*26-111insTG
NM_001204306.1:c.*26-112_*26-111insTG	NP_001191235.1:n.*26-112_*26-111insTG
NM_001204307.1:c.*26-112_*26-111insTG	NP_001191236.1:n.*26-112_*26-111insTG
XM_006714177.2:c.*40-112_*40-111insTG	XP_006714240.1:n.*40-112_*40-111insTG
XM_006714177.3:c.*40-112_*40-111insTG	XP_006714240.1:n.*40-112_*40-111insTG
NM_000583.4:c.*26-112_*26-111insTG MANE Select	NP_000574.2:n.*26-112_*26-111insTG