Canonical Allele Identifier: CA342755428

Gene: PKLR

Linked Data

• gnomAD v4: 1-155295439-C-T
• MyVariant Identifiers: chr1:g.155265230C>T (hg19) ; chr1:g.155295439C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155295439C>T , CM000663.2:g.155295439C>T	GRCh38
NC_000001.10:g.155265230C>T , CM000663.1:g.155265230C>T	GRCh37
NC_000001.9:g.153531854C>T	NCBI36
NG_011677.1:g.10996G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.505G>A MANE Select	ENSP00000339933.4:p.Gly169Arg
ENST00000434082.3:c.313G>A	ENSP00000398037.3:p.Gly105Arg
ENST00000342741.4:c.505G>A	ENSP00000339933.4:p.Gly169Arg
ENST00000392414.7:c.412G>A	ENSP00000376214.3:p.Gly138Arg
ENST00000434082.2:c.410G>A	ENSP00000398037.2:n.410G>A
NM_000298.5:c.505G>A	NP_000289.1:p.Gly169Arg
NM_181871.3:c.412G>A	NP_870986.1:p.Gly138Arg
XM_005245266.3:c.664G>A	XP_005245323.1:p.Gly222Arg
XM_006711386.2:c.313G>A	XP_006711449.1:p.Gly105Arg
XM_011509639.1:c.664G>A	XP_011507941.1:p.Gly222Arg
XM_011509640.1:c.313G>A	XP_011507942.1:p.Gly105Arg
NM_000298.6:c.505G>A MANE Select	NP_000289.1:p.Gly169Arg
XM_006711386.4:c.313G>A	XP_006711449.1:p.Gly105Arg
XM_011509640.3:c.313G>A	XP_011507942.1:p.Gly105Arg
XM_017001493.1:c.505G>A	XP_016856982.1:p.Gly169Arg
NM_181871.4:c.412G>A	NP_870986.1:p.Gly138Arg