Canonical Allele Identifier: CA639614084

Gene: UPK3A

Linked Data

• dbSNP Id: rs1350374973
• gnomAD v2: 22-45688996-G-T
• gnomAD v3: 22-45293115-G-T
• gnomAD v4: 22-45293115-G-T
• MyVariant Identifiers: chr22:g.45688996G>T (hg19) ; chr22:g.45293115G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.45293115G>T , CM000684.2:g.45293115G>T	GRCh38
NC_000022.10:g.45688996G>T , CM000684.1:g.45688996G>T	GRCh37
NC_000022.9:g.44067660G>T	NCBI36
NG_016203.1:g.13129G>T
NG_016203.2:g.13129G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000216211.9:c.572-66G>T MANE Select	ENSP00000216211.4:n.572-66G>T
ENST00000216211.8:c.572-66G>T	ENSP00000216211.4:n.572-66G>T
ENST00000396082.2:c.209-66G>T	ENSP00000379391.2:n.209-66G>T
NM_001167574.1:c.209-66G>T	NP_001161046.1:n.209-66G>T
NM_006953.3:c.572-66G>T	NP_008884.1:n.572-66G>T
XM_011530364.1:c.578-66G>T	XP_011528666.1:n.578-66G>T
XM_011530365.1:c.215-66G>T	XP_011528667.1:n.215-66G>T
NM_006953.4:c.572-66G>T MANE Select	NP_008884.1:n.572-66G>T
NM_001167574.2:c.209-66G>T	NP_001161046.1:n.209-66G>T