Canonical Allele Identifier: CA2657267311
Gene: UPK3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.45293415C>A , CM000684.2:g.45293415C>A GRCh38
NC_000022.10:g.45689296C>A , CM000684.1:g.45689296C>A GRCh37
NC_000022.9:g.44067960C>A NCBI36
NG_016203.1:g.13429C>A
NG_016203.2:g.13429C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216211.9:c.704+102C>A MANE Select ENSP00000216211.4:n.704+102C>A
ENST00000216211.8:c.704+102C>A ENSP00000216211.4:n.704+102C>A
ENST00000396082.2:c.341+102C>A ENSP00000379391.2:n.341+102C>A
NM_001167574.1:c.341+102C>A NP_001161046.1:n.341+102C>A
NM_006953.3:c.704+102C>A NP_008884.1:n.704+102C>A
XM_011530364.1:c.710+102C>A XP_011528666.1:n.710+102C>A
XM_011530365.1:c.347+102C>A XP_011528667.1:n.347+102C>A
NM_006953.4:c.704+102C>A MANE Select NP_008884.1:n.704+102C>A
NM_001167574.2:c.341+102C>A NP_001161046.1:n.341+102C>A