Canonical Allele Identifier: CA2408185539
Gene: UPK3A HGNC NCBI

Linked Data

dbSNP Id: rs2084175864

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.45293467G>C , CM000684.2:g.45293467G>C GRCh38
NC_000022.10:g.45689348G>C , CM000684.1:g.45689348G>C GRCh37
NC_000022.9:g.44068012G>C NCBI36
NG_016203.1:g.13481G>C
NG_016203.2:g.13481G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000216211.9:c.704+154G>C MANE Select ENSP00000216211.4:n.704+154G>C
ENST00000216211.8:c.704+154G>C ENSP00000216211.4:n.704+154G>C
ENST00000396082.2:c.341+154G>C ENSP00000379391.2:n.341+154G>C
NM_001167574.1:c.341+154G>C NP_001161046.1:n.341+154G>C
NM_006953.3:c.704+154G>C NP_008884.1:n.704+154G>C
XM_011530364.1:c.710+154G>C XP_011528666.1:n.710+154G>C
XM_011530365.1:c.347+154G>C XP_011528667.1:n.347+154G>C
NM_006953.4:c.704+154G>C MANE Select NP_008884.1:n.704+154G>C
NM_001167574.2:c.341+154G>C NP_001161046.1:n.341+154G>C