Canonical Allele Identifier: CA1467373185

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756749_71756753delinsCTTTG , CM000666.2:g.71756749_71756753delinsCTTTG	GRCh38
NC_000004.11:g.72622466_72622470delinsCTTTG , CM000666.1:g.72622466_72622470delinsCTTTG	GRCh37
NC_000004.10:g.72841330_72841334delinsCTTTG	NCBI36
NG_012837.2:g.53768_53772delinsCAAAG
NG_012837.3:g.53768_53772delinsCAAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.993_997delinsCAAAG MANE Select	ENSP00000273951.8:p.Asn331=
ENST00000273951.12:c.993_997delinsCAAAG	ENSP00000273951.8:p.Asn331=
ENST00000503472.5:n.877_881delinsCAAAG
ENST00000504199.5:c.1050_1054delinsCAAAG	ENSP00000421725.1:p.Asn350=
ENST00000509740.5:c.993_997delinsCAAAG	ENSP00000422664.1:p.Asn331=
ENST00000513476.5:c.993_997delinsCAAAG	ENSP00000426683.1:p.Asn331=
NM_000583.3:c.993_997delinsCAAAG	NP_000574.2:p.Asn331=
NM_001204306.1:c.993_997delinsCAAAG	NP_001191235.1:p.Asn331=
NM_001204307.1:c.1050_1054delinsCAAAG	NP_001191236.1:p.Asn350=
XM_006714177.2:c.993_997delinsCAAAG	XP_006714240.1:p.Asn331=
XM_006714177.3:c.993_997delinsCAAAG	XP_006714240.1:p.Asn331=
NM_000583.4:c.993_997delinsCAAAG MANE Select	NP_000574.2:p.Asn331=