Canonical Allele Identifier: CA894034845
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs769189064
MyVariant Identifiers: chr2:g.85773539_85773540insTA (hg19) chr2:g.85546416_85546417insTA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546416_85546417insTA , CM000664.2:g.85546416_85546417insTA GRCh38
NC_000002.11:g.85773539_85773540insTA , CM000664.1:g.85773539_85773540insTA GRCh37
NC_000002.10:g.85627050_85627051insTA NCBI36
NG_011811.2:g.20118_20119insTA
NG_029183.1:g.12439_12440insTA

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3517_*3518insTA MANE Select ENSP00000233838.3:n.*3517_*3518insTA
ENST00000233838.8:c.*3517_*3518insTA ENSP00000233838.3:n.*3517_*3518insTA
NM_000821.5:c.*3517_*3518insTA NP_000812.2:n.*3517_*3518insTA
NM_000821.6:c.*3517_*3518insTA NP_000812.2:n.*3517_*3518insTA
NM_001142269.2:c.*3517_*3518insTA NP_001135741.1:n.*3517_*3518insTA
NM_001142269.3:c.*3517_*3518insTA NP_001135741.1:n.*3517_*3518insTA
NM_000821.7:c.*3517_*3518insTA MANE Select NP_000812.2:n.*3517_*3518insTA
NM_001142269.4:c.*3517_*3518insTA NP_001135741.1:n.*3517_*3518insTA
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