Canonical Allele Identifier: CA2670941961

Gene: GC

Linked Data

• gnomAD v4: 4-71756782-CGGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756784_71756786del , CM000666.2:g.71756784_71756786del	GRCh38
NC_000004.11:g.72622501_72622503del , CM000666.1:g.72622501_72622503del	GRCh37
NC_000004.10:g.72841365_72841367del	NCBI36
NG_012837.2:g.53736_53738del
NG_012837.3:g.53736_53738del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.961_963del MANE Select	ENSP00000273951.8:p.Pro321del
ENST00000273951.12:c.961_963del	ENSP00000273951.8:p.Pro321del
ENST00000503472.5:n.845_847del
ENST00000504199.5:c.1018_1020del	ENSP00000421725.1:p.Pro340del
ENST00000509740.5:c.961_963del	ENSP00000422664.1:p.Pro321del
ENST00000513476.5:c.961_963del	ENSP00000426683.1:p.Pro321del
NM_000583.3:c.961_963del	NP_000574.2:p.Pro321del
NM_001204306.1:c.961_963del	NP_001191235.1:p.Pro321del
NM_001204307.1:c.1018_1020del	NP_001191236.1:p.Pro340del
XM_006714177.2:c.961_963del	XP_006714240.1:p.Pro321del
XM_006714177.3:c.961_963del	XP_006714240.1:p.Pro321del
NM_000583.4:c.961_963del MANE Select	NP_000574.2:p.Pro321del