Canonical Allele Identifier: CA2408185575
Gene: UPK3A HGNC NCBI

Linked Data

dbSNP Id: rs2084176258

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.45293532_45293557dup , CM000684.2:g.45293532_45293557dup GRCh38
NC_000022.10:g.45689413_45689438dup , CM000684.1:g.45689413_45689438dup GRCh37
NC_000022.9:g.44068077_44068102dup NCBI36
NG_016203.1:g.13546_13571dup
NG_016203.2:g.13546_13571dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000216211.9:c.704+219_704+244dup MANE Select ENSP00000216211.4:n.704+219_704+244dup
ENST00000216211.8:c.704+219_704+244dup ENSP00000216211.4:n.704+219_704+244dup
ENST00000396082.2:c.341+219_341+244dup ENSP00000379391.2:n.341+219_341+244dup
NM_001167574.1:c.341+219_341+244dup NP_001161046.1:n.341+219_341+244dup
NM_006953.3:c.704+219_704+244dup NP_008884.1:n.704+219_704+244dup
XM_011530364.1:c.710+219_710+244dup XP_011528666.1:n.710+219_710+244dup
XM_011530365.1:c.347+219_347+244dup XP_011528667.1:n.347+219_347+244dup
NM_006953.4:c.704+219_704+244dup MANE Select NP_008884.1:n.704+219_704+244dup
NM_001167574.2:c.341+219_341+244dup NP_001161046.1:n.341+219_341+244dup