Canonical Allele Identifier: CA1266820620
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546365_85546366delinsGT , CM000664.2:g.85546365_85546366delinsGT GRCh38
NC_000002.11:g.85773488_85773489delinsGT , CM000664.1:g.85773488_85773489delinsGT GRCh37
NC_000002.10:g.85626999_85627000delinsGT NCBI36
NG_011811.2:g.20169_20170delinsAC
NG_029183.1:g.12388_12389delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3568_*3569delinsAC MANE Select ENSP00000233838.3:n.*3568_*3569delinsAC
ENST00000233838.8:c.*3568_*3569delinsAC ENSP00000233838.3:n.*3568_*3569delinsAC
NM_000821.5:c.*3568_*3569delinsAC NP_000812.2:n.*3568_*3569delinsAC
NM_000821.6:c.*3568_*3569delinsAC NP_000812.2:n.*3568_*3569delinsAC
NM_001142269.2:c.*3568_*3569delinsAC NP_001135741.1:n.*3568_*3569delinsAC
NM_001142269.3:c.*3568_*3569delinsAC NP_001135741.1:n.*3568_*3569delinsAC
NM_000821.7:c.*3568_*3569delinsAC MANE Select NP_000812.2:n.*3568_*3569delinsAC
NM_001142269.4:c.*3568_*3569delinsAC NP_001135741.1:n.*3568_*3569delinsAC