Canonical Allele Identifier: CA342754330

Gene: PKLR

Linked Data

• gnomAD v4: 1-155294638-C-G
• MyVariant Identifiers: chr1:g.155264429C>G (hg19) ; chr1:g.155294638C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294638C>G , CM000663.2:g.155294638C>G	GRCh38
NC_000001.10:g.155264429C>G , CM000663.1:g.155264429C>G	GRCh37
NC_000001.9:g.153531053C>G	NCBI36
NG_011677.1:g.11797G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.809G>C MANE Select	ENSP00000339933.4:p.Arg270Pro
ENST00000342741.4:c.809G>C	ENSP00000339933.4:p.Arg270Pro
ENST00000392414.7:c.716G>C	ENSP00000376214.3:p.Arg239Pro
NM_000298.5:c.809G>C	NP_000289.1:p.Arg270Pro
NM_181871.3:c.716G>C	NP_870986.1:p.Arg239Pro
XM_005245266.3:c.968G>C	XP_005245323.1:p.Arg323Pro
XM_006711386.2:c.617G>C	XP_006711449.1:p.Arg206Pro
XM_011509639.1:c.968G>C	XP_011507941.1:p.Arg323Pro
XM_011509640.1:c.617G>C	XP_011507942.1:p.Arg206Pro
NM_000298.6:c.809G>C MANE Select	NP_000289.1:p.Arg270Pro
XM_006711386.4:c.617G>C	XP_006711449.1:p.Arg206Pro
XM_011509640.3:c.617G>C	XP_011507942.1:p.Arg206Pro
XM_017001493.1:c.809G>C	XP_016856982.1:p.Arg270Pro
NM_181871.4:c.716G>C	NP_870986.1:p.Arg239Pro