Canonical Allele Identifier: CA342753992

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155264345C>G (hg19) ; chr1:g.155294554C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294554C>G , CM000663.2:g.155294554C>G	GRCh38
NC_000001.10:g.155264345C>G , CM000663.1:g.155264345C>G	GRCh37
NC_000001.9:g.153530969C>G	NCBI36
NG_011677.1:g.11881G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.893G>C MANE Select	ENSP00000339933.4:p.Arg298Thr
ENST00000342741.4:c.893G>C	ENSP00000339933.4:p.Arg298Thr
ENST00000392414.7:c.800G>C	ENSP00000376214.3:p.Arg267Thr
NM_000298.5:c.893G>C	NP_000289.1:p.Arg298Thr
NM_181871.3:c.800G>C	NP_870986.1:p.Arg267Thr
XM_005245266.3:c.1052G>C	XP_005245323.1:p.Arg351Thr
XM_006711386.2:c.701G>C	XP_006711449.1:p.Arg234Thr
XM_011509639.1:c.1052G>C	XP_011507941.1:p.Arg351Thr
XM_011509640.1:c.701G>C	XP_011507942.1:p.Arg234Thr
NM_000298.6:c.893G>C MANE Select	NP_000289.1:p.Arg298Thr
XM_006711386.4:c.701G>C	XP_006711449.1:p.Arg234Thr
XM_011509640.3:c.701G>C	XP_011507942.1:p.Arg234Thr
XM_017001493.1:c.893G>C	XP_016856982.1:p.Arg298Thr
NM_181871.4:c.800G>C	NP_870986.1:p.Arg267Thr