Canonical Allele Identifier: CA1266821059
Gene: GGCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546584_85546585delinsCT , CM000664.2:g.85546584_85546585delinsCT GRCh38
NC_000002.11:g.85773707_85773708delinsCT , CM000664.1:g.85773707_85773708delinsCT GRCh37
NC_000002.10:g.85627218_85627219delinsCT NCBI36
NG_011811.2:g.19950_19951delinsAG
NG_029183.1:g.12607_12608delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3349_*3350delinsAG MANE Select ENSP00000233838.3:n.*3349_*3350delinsAG
ENST00000233838.8:c.*3349_*3350delinsAG ENSP00000233838.3:n.*3349_*3350delinsAG
NM_000821.5:c.*3349_*3350delinsAG NP_000812.2:n.*3349_*3350delinsAG
NM_000821.6:c.*3349_*3350delinsAG NP_000812.2:n.*3349_*3350delinsAG
NM_001142269.2:c.*3349_*3350delinsAG NP_001135741.1:n.*3349_*3350delinsAG
NM_001142269.3:c.*3349_*3350delinsAG NP_001135741.1:n.*3349_*3350delinsAG
NM_000821.7:c.*3349_*3350delinsAG MANE Select NP_000812.2:n.*3349_*3350delinsAG
NM_001142269.4:c.*3349_*3350delinsAG NP_001135741.1:n.*3349_*3350delinsAG
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