Canonical Allele Identifier: CA2670941965

Gene: GC

Linked Data

• gnomAD v4: 4-71756907-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756908del , CM000666.2:g.71756908del	GRCh38
NC_000004.11:g.72622625del , CM000666.1:g.72622625del	GRCh37
NC_000004.10:g.72841489del	NCBI36
NG_012837.2:g.53613del
NG_012837.3:g.53613del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.838del MANE Select	ENSP00000273951.8:p.Glu280AsnfsTer4
ENST00000273951.12:c.838del	ENSP00000273951.8:p.Glu280AsnfsTer4
ENST00000503472.5:n.722del
ENST00000504199.5:c.895del	ENSP00000421725.1:p.Glu299AsnfsTer4
ENST00000509740.5:c.838del	ENSP00000422664.1:p.Glu280AsnfsTer4
ENST00000513476.5:c.838del	ENSP00000426683.1:p.Glu280AsnfsTer4
NM_000583.3:c.838del	NP_000574.2:p.Glu280AsnfsTer4
NM_001204306.1:c.838del	NP_001191235.1:p.Glu280AsnfsTer4
NM_001204307.1:c.895del	NP_001191236.1:p.Glu299AsnfsTer4
XM_006714177.2:c.838del	XP_006714240.1:p.Glu280AsnfsTer4
XM_006714177.3:c.838del	XP_006714240.1:p.Glu280AsnfsTer4
NM_000583.4:c.838del MANE Select	NP_000574.2:p.Glu280AsnfsTer4