Canonical Allele Identifier: CA2706447329

Gene: GC

Linked Data

• dbSNP Id: rs2149296585

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756073_71756074del , CM000666.2:g.71756073_71756074del	GRCh38
NC_000004.11:g.72621790_72621791del , CM000666.1:g.72621790_72621791del	GRCh37
NC_000004.10:g.72840654_72840655del	NCBI36
NG_012837.2:g.54450_54451del
NG_012837.3:g.54450_54451del

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.1034+641_1034+642del MANE Select	ENSP00000273951.8:n.1034+641_1034+642del
ENST00000273951.12:c.1034+641_1034+642del	ENSP00000273951.8:n.1034+641_1034+642del
ENST00000503472.5:n.918+641_918+642del
ENST00000504199.5:c.1091+641_1091+642del	ENSP00000421725.1:n.1091+641_1091+642del
ENST00000509740.5:c.1034+641_1034+642del	ENSP00000422664.1:n.1034+641_1034+642del
ENST00000513476.5:c.1034+641_1034+642del	ENSP00000426683.1:n.1034+641_1034+642del
NM_000583.3:c.1034+641_1034+642del	NP_000574.2:n.1034+641_1034+642del
NM_001204306.1:c.1034+641_1034+642del	NP_001191235.1:n.1034+641_1034+642del
NM_001204307.1:c.1091+641_1091+642del	NP_001191236.1:n.1091+641_1091+642del
XM_006714177.2:c.1034+641_1034+642del	XP_006714240.1:n.1034+641_1034+642del
XM_006714177.3:c.1034+641_1034+642del	XP_006714240.1:n.1034+641_1034+642del
NM_000583.4:c.1034+641_1034+642del MANE Select	NP_000574.2:n.1034+641_1034+642del