Canonical Allele Identifier: CA439796266

Gene: GC

Linked Data

• dbSNP Id: rs1741858046
• MyVariant Identifiers: chr4:g.72624180_72624213del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71758464_71758497del , CM000666.2:g.71758464_71758497del	GRCh38
NC_000004.11:g.72624181_72624214del , CM000666.1:g.72624181_72624214del	GRCh37
NC_000004.10:g.72843045_72843078del	NCBI36
NG_012837.2:g.52025_52058del
NG_012837.3:g.52025_52058del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.702-325_702-292del MANE Select	ENSP00000273951.8:n.702-325_702-292del
ENST00000273951.12:c.702-325_702-292del	ENSP00000273951.8:n.702-325_702-292del
ENST00000503472.5:n.586-325_586-292del
ENST00000504199.5:c.759-325_759-292del	ENSP00000421725.1:n.759-325_759-292del
ENST00000509740.5:c.702-325_702-292del	ENSP00000422664.1:n.702-325_702-292del
ENST00000513476.5:c.702-325_702-292del	ENSP00000426683.1:n.702-325_702-292del
NM_000583.3:c.702-325_702-292del	NP_000574.2:n.702-325_702-292del
NM_001204306.1:c.702-325_702-292del	NP_001191235.1:n.702-325_702-292del
NM_001204307.1:c.759-325_759-292del	NP_001191236.1:n.759-325_759-292del
XM_006714177.2:c.702-325_702-292del	XP_006714240.1:n.702-325_702-292del
XM_006714177.3:c.702-325_702-292del	XP_006714240.1:n.702-325_702-292del
NM_000583.4:c.702-325_702-292del MANE Select	NP_000574.2:n.702-325_702-292del