Canonical Allele Identifier: CA2706446183

Gene: GC

Linked Data

• dbSNP Id: rs2149290630

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741877_71741878insTT , CM000666.2:g.71741877_71741878insTT	GRCh38
NC_000004.11:g.72607594_72607595insTT , CM000666.1:g.72607594_72607595insTT	GRCh37
NC_000004.10:g.72826458_72826459insTT	NCBI36
NG_012837.2:g.68643_68644insAA
NG_012837.3:g.68643_68644insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*26-8_*26-7insAA MANE Select	ENSP00000273951.8:n.*26-8_*26-7insAA
ENST00000273951.12:c.*26-8_*26-7insAA	ENSP00000273951.8:n.*26-8_*26-7insAA
ENST00000503364.5:n.124-8_124-7insAA
ENST00000503472.5:n.1335-8_1335-7insAA
ENST00000504199.5:c.*26-8_*26-7insAA	ENSP00000421725.1:n.*26-8_*26-7insAA
ENST00000509740.5:c.*274-8_*274-7insAA	ENSP00000422664.1:n.*274-8_*274-7insAA
ENST00000513476.5:c.1396-8_1396-7insAA	ENSP00000426683.1:n.1396-8_1396-7insAA
NM_000583.3:c.*26-8_*26-7insAA	NP_000574.2:n.*26-8_*26-7insAA
NM_001204306.1:c.*26-8_*26-7insAA	NP_001191235.1:n.*26-8_*26-7insAA
NM_001204307.1:c.*26-8_*26-7insAA	NP_001191236.1:n.*26-8_*26-7insAA
XM_006714177.2:c.*40-8_*40-7insAA	XP_006714240.1:n.*40-8_*40-7insAA
XM_006714177.3:c.*40-8_*40-7insAA	XP_006714240.1:n.*40-8_*40-7insAA
NM_000583.4:c.*26-8_*26-7insAA MANE Select	NP_000574.2:n.*26-8_*26-7insAA