Canonical Allele Identifier: CA2524549929

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756855_71756856del , CM000666.2:g.71756855_71756856del	GRCh38
NC_000004.11:g.72622572_72622573del , CM000666.1:g.72622572_72622573del	GRCh37
NC_000004.10:g.72841436_72841437del	NCBI36
NG_012837.2:g.53665_53666del
NG_012837.3:g.53665_53666del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.890_891del MANE Select	ENSP00000273951.8:p.Glu297GlyfsTer?
ENST00000273951.12:c.890_891del	ENSP00000273951.8:p.Glu297GlyfsTer?
ENST00000503472.5:n.774_775del
ENST00000504199.5:c.947_948del	ENSP00000421725.1:p.Glu316GlyfsTer?
ENST00000509740.5:c.890_891del	ENSP00000422664.1:p.Glu297GlyfsTer?
ENST00000513476.5:c.890_891del	ENSP00000426683.1:p.Glu297GlyfsTer?
NM_000583.3:c.890_891del	NP_000574.2:p.Glu297GlyfsTer?
NM_001204306.1:c.890_891del	NP_001191235.1:p.Glu297GlyfsTer?
NM_001204307.1:c.947_948del	NP_001191236.1:p.Glu316GlyfsTer?
XM_006714177.2:c.890_891del	XP_006714240.1:p.Glu297GlyfsTer?
XM_006714177.3:c.890_891del	XP_006714240.1:p.Glu297GlyfsTer?
NM_000583.4:c.890_891del MANE Select	NP_000574.2:p.Glu297GlyfsTer?