Canonical Allele Identifier: CA2657267279
Gene: UPK3A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.45293371T>C , CM000684.2:g.45293371T>C GRCh38
NC_000022.10:g.45689252T>C , CM000684.1:g.45689252T>C GRCh37
NC_000022.9:g.44067916T>C NCBI36
NG_016203.1:g.13385T>C
NG_016203.2:g.13385T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216211.9:c.704+58T>C MANE Select ENSP00000216211.4:n.704+58T>C
ENST00000216211.8:c.704+58T>C ENSP00000216211.4:n.704+58T>C
ENST00000396082.2:c.341+58T>C ENSP00000379391.2:n.341+58T>C
NM_001167574.1:c.341+58T>C NP_001161046.1:n.341+58T>C
NM_006953.3:c.704+58T>C NP_008884.1:n.704+58T>C
XM_011530364.1:c.710+58T>C XP_011528666.1:n.710+58T>C
XM_011530365.1:c.347+58T>C XP_011528667.1:n.347+58T>C
NM_006953.4:c.704+58T>C MANE Select NP_008884.1:n.704+58T>C
NM_001167574.2:c.341+58T>C NP_001161046.1:n.341+58T>C