Canonical Allele Identifier: CA2408185355
Gene: UPK3A HGNC NCBI

Linked Data

dbSNP Id: rs1601850468

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.45293138T>G , CM000684.2:g.45293138T>G GRCh38
NC_000022.10:g.45689019T>G , CM000684.1:g.45689019T>G GRCh37
NC_000022.9:g.44067683T>G NCBI36
NG_016203.1:g.13152T>G
NG_016203.2:g.13152T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000216211.9:c.572-43T>G MANE Select ENSP00000216211.4:n.572-43T>G
ENST00000216211.8:c.572-43T>G ENSP00000216211.4:n.572-43T>G
ENST00000396082.2:c.209-43T>G ENSP00000379391.2:n.209-43T>G
NM_001167574.1:c.209-43T>G NP_001161046.1:n.209-43T>G
NM_006953.3:c.572-43T>G NP_008884.1:n.572-43T>G
XM_011530364.1:c.578-43T>G XP_011528666.1:n.578-43T>G
XM_011530365.1:c.215-43T>G XP_011528667.1:n.215-43T>G
NM_006953.4:c.572-43T>G MANE Select NP_008884.1:n.572-43T>G
NM_001167574.2:c.209-43T>G NP_001161046.1:n.209-43T>G