Canonical Allele Identifier: CA342755945

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155265359A>C (hg19) ; chr1:g.155295568A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155295568A>C , CM000663.2:g.155295568A>C	GRCh38
NC_000001.10:g.155265359A>C , CM000663.1:g.155265359A>C	GRCh37
NC_000001.9:g.153531983A>C	NCBI36
NG_011677.1:g.10867T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342741.6:c.376T>G MANE Select	ENSP00000339933.4:p.Tyr126Asp
ENST00000434082.3:c.184T>G	ENSP00000398037.3:p.Tyr62Asp
ENST00000342741.4:c.376T>G	ENSP00000339933.4:p.Tyr126Asp
ENST00000392414.7:c.283T>G	ENSP00000376214.3:p.Tyr95Asp
ENST00000434082.2:c.281T>G	ENSP00000398037.2:n.281T>G
NM_000298.5:c.376T>G	NP_000289.1:p.Tyr126Asp
NM_181871.3:c.283T>G	NP_870986.1:p.Tyr95Asp
XM_005245266.3:c.535T>G	XP_005245323.1:p.Tyr179Asp
XM_006711386.2:c.184T>G	XP_006711449.1:p.Tyr62Asp
XM_011509639.1:c.535T>G	XP_011507941.1:p.Tyr179Asp
XM_011509640.1:c.184T>G	XP_011507942.1:p.Tyr62Asp
NM_000298.6:c.376T>G MANE Select	NP_000289.1:p.Tyr126Asp
XM_006711386.4:c.184T>G	XP_006711449.1:p.Tyr62Asp
XM_011509640.3:c.184T>G	XP_011507942.1:p.Tyr62Asp
XM_017001493.1:c.376T>G	XP_016856982.1:p.Tyr126Asp
NM_181871.4:c.283T>G	NP_870986.1:p.Tyr95Asp