Canonical Allele Identifier: CA1266821031

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546561_85546564delinsAAAG , CM000664.2:g.85546561_85546564delinsAAAG	GRCh38
NC_000002.11:g.85773684_85773687delinsAAAG , CM000664.1:g.85773684_85773687delinsAAAG	GRCh37
NC_000002.10:g.85627195_85627198delinsAAAG	NCBI36
NG_011811.2:g.19971_19974delinsCTTT
NG_029183.1:g.12584_12587delinsAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*3370_*3373delinsCTTT MANE Select	ENSP00000233838.3:n.*3370_*3373delinsCTTT
ENST00000233838.8:c.*3370_*3373delinsCTTT	ENSP00000233838.3:n.*3370_*3373delinsCTTT
NM_000821.5:c.*3370_*3373delinsCTTT	NP_000812.2:n.*3370_*3373delinsCTTT
NM_000821.6:c.*3370_*3373delinsCTTT	NP_000812.2:n.*3370_*3373delinsCTTT
NM_001142269.2:c.*3370_*3373delinsCTTT	NP_001135741.1:n.*3370_*3373delinsCTTT
NM_001142269.3:c.*3370_*3373delinsCTTT	NP_001135741.1:n.*3370_*3373delinsCTTT
NM_000821.7:c.*3370_*3373delinsCTTT MANE Select	NP_000812.2:n.*3370_*3373delinsCTTT
NM_001142269.4:c.*3370_*3373delinsCTTT	NP_001135741.1:n.*3370_*3373delinsCTTT