Canonical Allele Identifier: CA421245966

Gene: PKLR

Linked Data

• gnomAD v4: 1-155294385-C-T
• MyVariant Identifiers: chr1:g.155264176C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294385C>T , CM000663.2:g.155294385C>T	GRCh38
NC_000001.10:g.155264176C>T , CM000663.1:g.155264176C>T	GRCh37
NC_000001.9:g.153530800C>T	NCBI36
NG_011677.1:g.12050G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.966G>A MANE Select	ENSP00000339933.4:p.Arg322=
ENST00000342741.4:c.966G>A	ENSP00000339933.4:p.Arg322=
ENST00000392414.7:c.873G>A	ENSP00000376214.3:p.Arg291=
NM_000298.5:c.966G>A	NP_000289.1:p.Arg322=
NM_181871.3:c.873G>A	NP_870986.1:p.Arg291=
XM_005245266.3:c.1125G>A	XP_005245323.1:p.Arg375=
XM_006711386.2:c.774G>A	XP_006711449.1:p.Arg258=
XM_011509639.1:c.1125G>A	XP_011507941.1:p.Arg375=
XM_011509640.1:c.774G>A	XP_011507942.1:p.Arg258=
NM_000298.6:c.966G>A MANE Select	NP_000289.1:p.Arg322=
XM_006711386.4:c.774G>A	XP_006711449.1:p.Arg258=
XM_011509640.3:c.774G>A	XP_011507942.1:p.Arg258=
XM_017001493.1:c.966G>A	XP_016856982.1:p.Arg322=
NM_181871.4:c.873G>A	NP_870986.1:p.Arg291=