Canonical Allele Identifier: CA342754569

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155264481T>C (hg19) ; chr1:g.155294690T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294690T>C , CM000663.2:g.155294690T>C	GRCh38
NC_000001.10:g.155264481T>C , CM000663.1:g.155264481T>C	GRCh37
NC_000001.9:g.153531105T>C	NCBI36
NG_011677.1:g.11745A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.757A>G MANE Select	ENSP00000339933.4:p.Asn253Asp
ENST00000342741.4:c.757A>G	ENSP00000339933.4:p.Asn253Asp
ENST00000392414.7:c.664A>G	ENSP00000376214.3:p.Asn222Asp
NM_000298.5:c.757A>G	NP_000289.1:p.Asn253Asp
NM_181871.3:c.664A>G	NP_870986.1:p.Asn222Asp
XM_005245266.3:c.916A>G	XP_005245323.1:p.Asn306Asp
XM_006711386.2:c.565A>G	XP_006711449.1:p.Asn189Asp
XM_011509639.1:c.916A>G	XP_011507941.1:p.Asn306Asp
XM_011509640.1:c.565A>G	XP_011507942.1:p.Asn189Asp
NM_000298.6:c.757A>G MANE Select	NP_000289.1:p.Asn253Asp
XM_006711386.4:c.565A>G	XP_006711449.1:p.Asn189Asp
XM_011509640.3:c.565A>G	XP_011507942.1:p.Asn189Asp
XM_017001493.1:c.757A>G	XP_016856982.1:p.Asn253Asp
NM_181871.4:c.664A>G	NP_870986.1:p.Asn222Asp