Canonical Allele Identifier: CA1467373253

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756889_71756891delinsCAG , CM000666.2:g.71756889_71756891delinsCAG	GRCh38
NC_000004.11:g.72622606_72622608delinsCAG , CM000666.1:g.72622606_72622608delinsCAG	GRCh37
NC_000004.10:g.72841470_72841472delinsCAG	NCBI36
NG_012837.2:g.53630_53632delinsCTG
NG_012837.3:g.53630_53632delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.855_857delinsCTG MANE Select	ENSP00000273951.8:p.Leu285=
ENST00000273951.12:c.855_857delinsCTG	ENSP00000273951.8:p.Leu285=
ENST00000503472.5:n.739_741delinsCTG
ENST00000504199.5:c.912_914delinsCTG	ENSP00000421725.1:p.Leu304=
ENST00000509740.5:c.855_857delinsCTG	ENSP00000422664.1:p.Leu285=
ENST00000513476.5:c.855_857delinsCTG	ENSP00000426683.1:p.Leu285=
NM_000583.3:c.855_857delinsCTG	NP_000574.2:p.Leu285=
NM_001204306.1:c.855_857delinsCTG	NP_001191235.1:p.Leu285=
NM_001204307.1:c.912_914delinsCTG	NP_001191236.1:p.Leu304=
XM_006714177.2:c.855_857delinsCTG	XP_006714240.1:p.Leu285=
XM_006714177.3:c.855_857delinsCTG	XP_006714240.1:p.Leu285=
NM_000583.4:c.855_857delinsCTG MANE Select	NP_000574.2:p.Leu285=