Canonical Allele Identifier: CA2408185569
Gene: UPK3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.45293523G= , CM000684.2:g.45293523G= GRCh38
NC_000022.10:g.45689404G= , CM000684.1:g.45689404G= GRCh37
NC_000022.9:g.44068068G= NCBI36
NG_016203.1:g.13537G=
NG_016203.2:g.13537G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000216211.9:c.704+210G= MANE Select ENSP00000216211.4:n.704+210G=
ENST00000216211.8:c.704+210G= ENSP00000216211.4:n.704+210G=
ENST00000396082.2:c.341+210G= ENSP00000379391.2:n.341+210G=
NM_001167574.1:c.341+210G= NP_001161046.1:n.341+210G=
NM_006953.3:c.704+210G= NP_008884.1:n.704+210G=
XM_011530364.1:c.710+210G= XP_011528666.1:n.710+210G=
XM_011530365.1:c.347+210G= XP_011528667.1:n.347+210G=
NM_006953.4:c.704+210G= MANE Select NP_008884.1:n.704+210G=
NM_001167574.2:c.341+210G= NP_001161046.1:n.341+210G=