Canonical Allele Identifier: CA342754785

Gene: PKLR

Linked Data

• gnomAD v4: 1-155294732-G-T
• MyVariant Identifiers: chr1:g.155264523G>T (hg19) ; chr1:g.155294732G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294732G>T , CM000663.2:g.155294732G>T	GRCh38
NC_000001.10:g.155264523G>T , CM000663.1:g.155264523G>T	GRCh37
NC_000001.9:g.153531147G>T	NCBI36
NG_011677.1:g.11703C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342741.6:c.715C>A MANE Select	ENSP00000339933.4:p.Gln239Lys
ENST00000342741.4:c.715C>A	ENSP00000339933.4:p.Gln239Lys
ENST00000392414.7:c.622C>A	ENSP00000376214.3:p.Gln208Lys
NM_000298.5:c.715C>A	NP_000289.1:p.Gln239Lys
NM_181871.3:c.622C>A	NP_870986.1:p.Gln208Lys
XM_005245266.3:c.874C>A	XP_005245323.1:p.Gln292Lys
XM_006711386.2:c.523C>A	XP_006711449.1:p.Gln175Lys
XM_011509639.1:c.874C>A	XP_011507941.1:p.Gln292Lys
XM_011509640.1:c.523C>A	XP_011507942.1:p.Gln175Lys
NM_000298.6:c.715C>A MANE Select	NP_000289.1:p.Gln239Lys
XM_006711386.4:c.523C>A	XP_006711449.1:p.Gln175Lys
XM_011509640.3:c.523C>A	XP_011507942.1:p.Gln175Lys
XM_017001493.1:c.715C>A	XP_016856982.1:p.Gln239Lys
NM_181871.4:c.622C>A	NP_870986.1:p.Gln208Lys