Canonical Allele Identifier: CA342754362

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155264436C>T (hg19) ; chr1:g.155294645C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294645C>T , CM000663.2:g.155294645C>T	GRCh38
NC_000001.10:g.155264436C>T , CM000663.1:g.155264436C>T	GRCh37
NC_000001.9:g.153531060C>T	NCBI36
NG_011677.1:g.11790G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.802G>A MANE Select	ENSP00000339933.4:p.Asp268Asn
ENST00000342741.4:c.802G>A	ENSP00000339933.4:p.Asp268Asn
ENST00000392414.7:c.709G>A	ENSP00000376214.3:p.Asp237Asn
NM_000298.5:c.802G>A	NP_000289.1:p.Asp268Asn
NM_181871.3:c.709G>A	NP_870986.1:p.Asp237Asn
XM_005245266.3:c.961G>A	XP_005245323.1:p.Asp321Asn
XM_006711386.2:c.610G>A	XP_006711449.1:p.Asp204Asn
XM_011509639.1:c.961G>A	XP_011507941.1:p.Asp321Asn
XM_011509640.1:c.610G>A	XP_011507942.1:p.Asp204Asn
NM_000298.6:c.802G>A MANE Select	NP_000289.1:p.Asp268Asn
XM_006711386.4:c.610G>A	XP_006711449.1:p.Asp204Asn
XM_011509640.3:c.610G>A	XP_011507942.1:p.Asp204Asn
XM_017001493.1:c.802G>A	XP_016856982.1:p.Asp268Asn
NM_181871.4:c.709G>A	NP_870986.1:p.Asp237Asn