Canonical Allele Identifier: CA1266820830

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546437_85546439delinsCTG , CM000664.2:g.85546437_85546439delinsCTG	GRCh38
NC_000002.11:g.85773560_85773562delinsCTG , CM000664.1:g.85773560_85773562delinsCTG	GRCh37
NC_000002.10:g.85627071_85627073delinsCTG	NCBI36
NG_011811.2:g.20096_20098delinsCAG
NG_029183.1:g.12460_12462delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*3495_*3497delinsCAG MANE Select	ENSP00000233838.3:n.*3495_*3497delinsCAG
ENST00000233838.8:c.*3495_*3497delinsCAG	ENSP00000233838.3:n.*3495_*3497delinsCAG
NM_000821.5:c.*3495_*3497delinsCAG	NP_000812.2:n.*3495_*3497delinsCAG
NM_000821.6:c.*3495_*3497delinsCAG	NP_000812.2:n.*3495_*3497delinsCAG
NM_001142269.2:c.*3495_*3497delinsCAG	NP_001135741.1:n.*3495_*3497delinsCAG
NM_001142269.3:c.*3495_*3497delinsCAG	NP_001135741.1:n.*3495_*3497delinsCAG
NM_000821.7:c.*3495_*3497delinsCAG MANE Select	NP_000812.2:n.*3495_*3497delinsCAG
NM_001142269.4:c.*3495_*3497delinsCAG	NP_001135741.1:n.*3495_*3497delinsCAG