Canonical Allele Identifier: CA342754000

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155264348A>T (hg19) ; chr1:g.155294557A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294557A>T , CM000663.2:g.155294557A>T	GRCh38
NC_000001.10:g.155264348A>T , CM000663.1:g.155264348A>T	GRCh37
NC_000001.9:g.153530972A>T	NCBI36
NG_011677.1:g.11878T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.890T>A MANE Select	ENSP00000339933.4:p.Val297Asp
ENST00000342741.4:c.890T>A	ENSP00000339933.4:p.Val297Asp
ENST00000392414.7:c.797T>A	ENSP00000376214.3:p.Val266Asp
NM_000298.5:c.890T>A	NP_000289.1:p.Val297Asp
NM_181871.3:c.797T>A	NP_870986.1:p.Val266Asp
XM_005245266.3:c.1049T>A	XP_005245323.1:p.Val350Asp
XM_006711386.2:c.698T>A	XP_006711449.1:p.Val233Asp
XM_011509639.1:c.1049T>A	XP_011507941.1:p.Val350Asp
XM_011509640.1:c.698T>A	XP_011507942.1:p.Val233Asp
NM_000298.6:c.890T>A MANE Select	NP_000289.1:p.Val297Asp
XM_006711386.4:c.698T>A	XP_006711449.1:p.Val233Asp
XM_011509640.3:c.698T>A	XP_011507942.1:p.Val233Asp
XM_017001493.1:c.890T>A	XP_016856982.1:p.Val297Asp
NM_181871.4:c.797T>A	NP_870986.1:p.Val266Asp