Canonical Allele Identifier: CA249381385
Gene: KPNA3 HGNC NCBI

Linked Data

dbSNP Id: rs1004171777
MyVariant Identifiers: chr13:g.49732103A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.49732103A>G , CM000675.2:g.49732103A>G GRCh38
NC_000013.10:g.50306239A>G , CM000675.1:g.50306239A>G GRCh37
NC_000013.9:g.49204240A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261667.8:c.383+268T>C MANE Select ENSP00000261667.3:n.383+268T>C
ENST00000261667.7:c.383+268T>C ENSP00000261667.3:n.383+268T>C
NM_002267.3:c.383+268T>C NP_002258.2:n.383+268T>C
XM_017020561.1:c.311+268T>C XP_016876050.1:n.311+268T>C
NM_002267.4:c.383+268T>C MANE Select NP_002258.2:n.383+268T>C
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