Canonical Allele Identifier: CA1266821074

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546602_85546604delinsCAG , CM000664.2:g.85546602_85546604delinsCAG	GRCh38
NC_000002.11:g.85773725_85773727delinsCAG , CM000664.1:g.85773725_85773727delinsCAG	GRCh37
NC_000002.10:g.85627236_85627238delinsCAG	NCBI36
NG_011811.2:g.19931_19933delinsCTG
NG_029183.1:g.12625_12627delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*3330_*3332delinsCTG MANE Select	ENSP00000233838.3:n.*3330_*3332delinsCTG
ENST00000233838.8:c.*3330_*3332delinsCTG	ENSP00000233838.3:n.*3330_*3332delinsCTG
NM_000821.5:c.*3330_*3332delinsCTG	NP_000812.2:n.*3330_*3332delinsCTG
NM_000821.6:c.*3330_*3332delinsCTG	NP_000812.2:n.*3330_*3332delinsCTG
NM_001142269.2:c.*3330_*3332delinsCTG	NP_001135741.1:n.*3330_*3332delinsCTG
NM_001142269.3:c.*3330_*3332delinsCTG	NP_001135741.1:n.*3330_*3332delinsCTG
NM_000821.7:c.*3330_*3332delinsCTG MANE Select	NP_000812.2:n.*3330_*3332delinsCTG
NM_001142269.4:c.*3330_*3332delinsCTG	NP_001135741.1:n.*3330_*3332delinsCTG