Canonical Allele Identifier: CA421245682

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155264424G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294633G>A , CM000663.2:g.155294633G>A	GRCh38
NC_000001.10:g.155264424G>A , CM000663.1:g.155264424G>A	GRCh37
NC_000001.9:g.153531048G>A	NCBI36
NG_011677.1:g.11802C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.814C>T MANE Select	ENSP00000339933.4:p.Leu272=
ENST00000342741.4:c.814C>T	ENSP00000339933.4:p.Leu272=
ENST00000392414.7:c.721C>T	ENSP00000376214.3:p.Leu241=
NM_000298.5:c.814C>T	NP_000289.1:p.Leu272=
NM_181871.3:c.721C>T	NP_870986.1:p.Leu241=
XM_005245266.3:c.973C>T	XP_005245323.1:p.Leu325=
XM_006711386.2:c.622C>T	XP_006711449.1:p.Leu208=
XM_011509639.1:c.973C>T	XP_011507941.1:p.Leu325=
XM_011509640.1:c.622C>T	XP_011507942.1:p.Leu208=
NM_000298.6:c.814C>T MANE Select	NP_000289.1:p.Leu272=
XM_006711386.4:c.622C>T	XP_006711449.1:p.Leu208=
XM_011509640.3:c.622C>T	XP_011507942.1:p.Leu208=
XM_017001493.1:c.814C>T	XP_016856982.1:p.Leu272=
NM_181871.4:c.721C>T	NP_870986.1:p.Leu241=