Canonical Allele Identifier: CA2670941962

Gene: GC

Linked Data

• gnomAD v4: 4-71756807-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756808dup , CM000666.2:g.71756808dup	GRCh38
NC_000004.11:g.72622525dup , CM000666.1:g.72622525dup	GRCh37
NC_000004.10:g.72841389dup	NCBI36
NG_012837.2:g.53713dup
NG_012837.3:g.53713dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.938dup MANE Select	ENSP00000273951.8:p.Tyr313Ter
ENST00000273951.12:c.938dup	ENSP00000273951.8:p.Tyr313Ter
ENST00000503472.5:n.822dup
ENST00000504199.5:c.995dup	ENSP00000421725.1:p.Tyr332Ter
ENST00000509740.5:c.938dup	ENSP00000422664.1:p.Tyr313Ter
ENST00000513476.5:c.938dup	ENSP00000426683.1:p.Tyr313Ter
NM_000583.3:c.938dup	NP_000574.2:p.Tyr313Ter
NM_001204306.1:c.938dup	NP_001191235.1:p.Tyr313Ter
NM_001204307.1:c.995dup	NP_001191236.1:p.Tyr332Ter
XM_006714177.2:c.938dup	XP_006714240.1:p.Tyr313Ter
XM_006714177.3:c.938dup	XP_006714240.1:p.Tyr313Ter
NM_000583.4:c.938dup MANE Select	NP_000574.2:p.Tyr313Ter