Canonical Allele Identifier: CA1266820006
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545969_85545970delinsAC , CM000664.2:g.85545969_85545970delinsAC GRCh38
NC_000002.11:g.85773092_85773093delinsAC , CM000664.1:g.85773092_85773093delinsAC GRCh37
NC_000002.10:g.85626603_85626604delinsAC NCBI36
NG_011811.2:g.20565_20566delinsGT
NG_029183.1:g.11992_11993delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3964_*3965delinsGT MANE Select ENSP00000233838.3:n.*3964_*3965delinsGT
ENST00000233838.8:c.*3964_*3965delinsGT ENSP00000233838.3:n.*3964_*3965delinsGT
NM_000821.5:c.*3964_*3965delinsGT NP_000812.2:n.*3964_*3965delinsGT
NM_000821.6:c.*3964_*3965delinsGT NP_000812.2:n.*3964_*3965delinsGT
NM_001142269.2:c.*3964_*3965delinsGT NP_001135741.1:n.*3964_*3965delinsGT
NM_001142269.3:c.*3964_*3965delinsGT NP_001135741.1:n.*3964_*3965delinsGT
NM_000821.7:c.*3964_*3965delinsGT MANE Select NP_000812.2:n.*3964_*3965delinsGT
NM_001142269.4:c.*3964_*3965delinsGT NP_001135741.1:n.*3964_*3965delinsGT