Canonical Allele Identifier: CA955896789
Gene: KPNA3 HGNC NCBI

Linked Data

dbSNP Id: rs1566342750
gnomAD v3: 13-49731995-T-C
gnomAD v4: 13-49731995-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.49731995T>C , CM000675.2:g.49731995T>C GRCh38
NC_000013.10:g.50306131T>C , CM000675.1:g.50306131T>C GRCh37
NC_000013.9:g.49204132T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261667.8:c.383+376A>G MANE Select ENSP00000261667.3:n.383+376A>G
ENST00000261667.7:c.383+376A>G ENSP00000261667.3:n.383+376A>G
NM_002267.3:c.383+376A>G NP_002258.2:n.383+376A>G
XM_017020561.1:c.311+376A>G XP_016876050.1:n.311+376A>G
NM_002267.4:c.383+376A>G MANE Select NP_002258.2:n.383+376A>G
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