Canonical Allele Identifier: CA342754363

Gene: PKLR

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.802G>T MANE Select	ENSP00000339933.4:p.Asp268Tyr
ENST00000342741.4:c.802G>T	ENSP00000339933.4:p.Asp268Tyr
ENST00000392414.7:c.709G>T	ENSP00000376214.3:p.Asp237Tyr
NM_000298.5:c.802G>T	NP_000289.1:p.Asp268Tyr
NM_181871.3:c.709G>T	NP_870986.1:p.Asp237Tyr
XM_005245266.3:c.961G>T	XP_005245323.1:p.Asp321Tyr
XM_006711386.2:c.610G>T	XP_006711449.1:p.Asp204Tyr
XM_011509639.1:c.961G>T	XP_011507941.1:p.Asp321Tyr
XM_011509640.1:c.610G>T	XP_011507942.1:p.Asp204Tyr
NM_000298.6:c.802G>T MANE Select	NP_000289.1:p.Asp268Tyr
XM_006711386.4:c.610G>T	XP_006711449.1:p.Asp204Tyr
XM_011509640.3:c.610G>T	XP_011507942.1:p.Asp204Tyr
XM_017001493.1:c.802G>T	XP_016856982.1:p.Asp268Tyr
NM_181871.4:c.709G>T	NP_870986.1:p.Asp237Tyr