Canonical Allele Identifier: CA342753885

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155264321T>G (hg19) ; chr1:g.155294530T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294530T>G , CM000663.2:g.155294530T>G	GRCh38
NC_000001.10:g.155264321T>G , CM000663.1:g.155264321T>G	GRCh37
NC_000001.9:g.153530945T>G	NCBI36
NG_011677.1:g.11905A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.917A>C MANE Select	ENSP00000339933.4:p.His306Pro
ENST00000342741.4:c.917A>C	ENSP00000339933.4:p.His306Pro
ENST00000392414.7:c.824A>C	ENSP00000376214.3:p.His275Pro
NM_000298.5:c.917A>C	NP_000289.1:p.His306Pro
NM_181871.3:c.824A>C	NP_870986.1:p.His275Pro
XM_005245266.3:c.1076A>C	XP_005245323.1:p.His359Pro
XM_006711386.2:c.725A>C	XP_006711449.1:p.His242Pro
XM_011509639.1:c.1076A>C	XP_011507941.1:p.His359Pro
XM_011509640.1:c.725A>C	XP_011507942.1:p.His242Pro
NM_000298.6:c.917A>C MANE Select	NP_000289.1:p.His306Pro
XM_006711386.4:c.725A>C	XP_006711449.1:p.His242Pro
XM_011509640.3:c.725A>C	XP_011507942.1:p.His242Pro
XM_017001493.1:c.917A>C	XP_016856982.1:p.His306Pro
NM_181871.4:c.824A>C	NP_870986.1:p.His275Pro