Canonical Allele Identifier: CA411879428

Gene: UPK3A

Linked Data

• MyVariant Identifiers: chr22:g.45689151T>G (hg19) ; chr22:g.45293270T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.45293270T>G , CM000684.2:g.45293270T>G	GRCh38
NC_000022.10:g.45689151T>G , CM000684.1:g.45689151T>G	GRCh37
NC_000022.9:g.44067815T>G	NCBI36
NG_016203.1:g.13284T>G
NG_016203.2:g.13284T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216211.9:c.661T>G MANE Select	ENSP00000216211.4:p.Phe221Val
ENST00000216211.8:c.661T>G	ENSP00000216211.4:p.Phe221Val
ENST00000396082.2:c.298T>G	ENSP00000379391.2:p.Phe100Val
NM_001167574.1:c.298T>G	NP_001161046.1:p.Phe100Val
NM_006953.3:c.661T>G	NP_008884.1:p.Phe221Val
XM_011530364.1:c.667T>G	XP_011528666.1:p.Phe223Val
XM_011530365.1:c.304T>G	XP_011528667.1:p.Phe102Val
NM_006953.4:c.661T>G MANE Select	NP_008884.1:p.Phe221Val
NM_001167574.2:c.298T>G	NP_001161046.1:p.Phe100Val