Canonical Allele Identifier: CA2706446070

Gene: GC

Linked Data

• dbSNP Id: rs2149290624

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741874_71741875del , CM000666.2:g.71741874_71741875del	GRCh38
NC_000004.11:g.72607591_72607592del , CM000666.1:g.72607591_72607592del	GRCh37
NC_000004.10:g.72826455_72826456del	NCBI36
NG_012837.2:g.68646_68647del
NG_012837.3:g.68646_68647del

Transcript Alleles

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