Canonical Allele Identifier: CA51729725
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs67176848
MyVariant Identifiers: chr2:g.85773655_85773656insTG (hg19) chr2:g.85546532_85546533insTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546532_85546533insTG , CM000664.2:g.85546532_85546533insTG GRCh38
NC_000002.11:g.85773655_85773656insTG , CM000664.1:g.85773655_85773656insTG GRCh37
NC_000002.10:g.85627166_85627167insTG NCBI36
NG_011811.2:g.20002_20003insCA
NG_029183.1:g.12555_12556insTG

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3401_*3402insCA MANE Select ENSP00000233838.3:n.*3401_*3402insCA
ENST00000233838.8:c.*3401_*3402insCA ENSP00000233838.3:n.*3401_*3402insCA
NM_000821.5:c.*3401_*3402insCA NP_000812.2:n.*3401_*3402insCA
NM_000821.6:c.*3401_*3402insCA NP_000812.2:n.*3401_*3402insCA
NM_001142269.2:c.*3401_*3402insCA NP_001135741.1:n.*3401_*3402insCA
NM_001142269.3:c.*3401_*3402insCA NP_001135741.1:n.*3401_*3402insCA
NM_000821.7:c.*3401_*3402insCA MANE Select NP_000812.2:n.*3401_*3402insCA
NM_001142269.4:c.*3401_*3402insCA NP_001135741.1:n.*3401_*3402insCA
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