Canonical Allele Identifier: CA1200112626

Gene: PKLR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155295453G= , CM000663.2:g.155295453G=	GRCh38
NC_000001.10:g.155265244G= , CM000663.1:g.155265244G=	GRCh37
NC_000001.9:g.153531868G=	NCBI36
NG_011677.1:g.10982C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.491C= MANE Select	ENSP00000339933.4:p.Thr164=
ENST00000434082.3:c.299C=	ENSP00000398037.3:p.Thr100=
ENST00000342741.4:c.491C=	ENSP00000339933.4:p.Thr164=
ENST00000392414.7:c.398C=	ENSP00000376214.3:p.Thr133=
ENST00000434082.2:c.396C=	ENSP00000398037.2:n.396C=
NM_000298.5:c.491C=	NP_000289.1:p.Thr164=
NM_181871.3:c.398C=	NP_870986.1:p.Thr133=
XM_005245266.3:c.650C=	XP_005245323.1:p.Thr217=
XM_006711386.2:c.299C=	XP_006711449.1:p.Thr100=
XM_011509639.1:c.650C=	XP_011507941.1:p.Thr217=
XM_011509640.1:c.299C=	XP_011507942.1:p.Thr100=
NM_000298.6:c.491C= MANE Select	NP_000289.1:p.Thr164=
XM_006711386.4:c.299C=	XP_006711449.1:p.Thr100=
XM_011509640.3:c.299C=	XP_011507942.1:p.Thr100=
XM_017001493.1:c.491C=	XP_016856982.1:p.Thr164=
NM_181871.4:c.398C=	NP_870986.1:p.Thr133=