Canonical Allele Identifier: CA1266819915

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85545879_85545881delinsCAG , CM000664.2:g.85545879_85545881delinsCAG	GRCh38
NC_000002.11:g.85773002_85773004delinsCAG , CM000664.1:g.85773002_85773004delinsCAG	GRCh37
NC_000002.10:g.85626513_85626515delinsCAG	NCBI36
NG_011811.2:g.20654_20656delinsCTG
NG_029183.1:g.11902_11904delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000233838.9:c.*4053_*4055delinsCTG MANE Select	ENSP00000233838.3:n.*4053_*4055delinsCTG
ENST00000233838.8:c.*4053_*4055delinsCTG	ENSP00000233838.3:n.*4053_*4055delinsCTG
NM_000821.5:c.*4053_*4055delinsCTG	NP_000812.2:n.*4053_*4055delinsCTG
NM_000821.6:c.*4053_*4055delinsCTG	NP_000812.2:n.*4053_*4055delinsCTG
NM_001142269.2:c.*4053_*4055delinsCTG	NP_001135741.1:n.*4053_*4055delinsCTG
NM_001142269.3:c.*4053_*4055delinsCTG	NP_001135741.1:n.*4053_*4055delinsCTG
NM_000821.7:c.*4053_*4055delinsCTG MANE Select	NP_000812.2:n.*4053_*4055delinsCTG
NM_001142269.4:c.*4053_*4055delinsCTG	NP_001135741.1:n.*4053_*4055delinsCTG