Canonical Allele Identifier: CA411879362
Gene: UPK3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.45293255G>A , CM000684.2:g.45293255G>A GRCh38
NC_000022.10:g.45689136G>A , CM000684.1:g.45689136G>A GRCh37
NC_000022.9:g.44067800G>A NCBI36
NG_016203.1:g.13269G>A
NG_016203.2:g.13269G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000216211.9:c.646G>A MANE Select ENSP00000216211.4:p.Gly216Ser
ENST00000216211.8:c.646G>A ENSP00000216211.4:p.Gly216Ser
ENST00000396082.2:c.283G>A ENSP00000379391.2:p.Gly95Ser
NM_001167574.1:c.283G>A NP_001161046.1:p.Gly95Ser
NM_006953.3:c.646G>A NP_008884.1:p.Gly216Ser
XM_011530364.1:c.652G>A XP_011528666.1:p.Gly218Ser
XM_011530365.1:c.289G>A XP_011528667.1:p.Gly97Ser
NM_006953.4:c.646G>A MANE Select NP_008884.1:p.Gly216Ser
NM_001167574.2:c.283G>A NP_001161046.1:p.Gly95Ser