Canonical Allele Identifier: CA421245757

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155264478A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294687A>G , CM000663.2:g.155294687A>G	GRCh38
NC_000001.10:g.155264478A>G , CM000663.1:g.155264478A>G	GRCh37
NC_000001.9:g.153531102A>G	NCBI36
NG_011677.1:g.11748T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.760T>C MANE Select	ENSP00000339933.4:p.Leu254=
ENST00000342741.4:c.760T>C	ENSP00000339933.4:p.Leu254=
ENST00000392414.7:c.667T>C	ENSP00000376214.3:p.Leu223=
NM_000298.5:c.760T>C	NP_000289.1:p.Leu254=
NM_181871.3:c.667T>C	NP_870986.1:p.Leu223=
XM_005245266.3:c.919T>C	XP_005245323.1:p.Leu307=
XM_006711386.2:c.568T>C	XP_006711449.1:p.Leu190=
XM_011509639.1:c.919T>C	XP_011507941.1:p.Leu307=
XM_011509640.1:c.568T>C	XP_011507942.1:p.Leu190=
NM_000298.6:c.760T>C MANE Select	NP_000289.1:p.Leu254=
XM_006711386.4:c.568T>C	XP_006711449.1:p.Leu190=
XM_011509640.3:c.568T>C	XP_011507942.1:p.Leu190=
XM_017001493.1:c.760T>C	XP_016856982.1:p.Leu254=
NM_181871.4:c.667T>C	NP_870986.1:p.Leu223=