Canonical Allele Identifier: CA655069125
Gene: KPNA3 HGNC NCBI

Linked Data

dbSNP Id: rs1325806113
COSMIC: COSN23406771
MyVariant Identifiers: chr13:g.50306310C>A (hg19) chr13:g.49732174C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.49732174C>A , CM000675.2:g.49732174C>A GRCh38
NC_000013.10:g.50306310C>A , CM000675.1:g.50306310C>A GRCh37
NC_000013.9:g.49204311C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261667.8:c.383+197G>T MANE Select ENSP00000261667.3:n.383+197G>T
ENST00000261667.7:c.383+197G>T ENSP00000261667.3:n.383+197G>T
NM_002267.3:c.383+197G>T NP_002258.2:n.383+197G>T
XM_017020561.1:c.311+197G>T XP_016876050.1:n.311+197G>T
NM_002267.4:c.383+197G>T MANE Select NP_002258.2:n.383+197G>T
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