Canonical Allele Identifier: CA1200112276

Gene: PKLR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294721G= , CM000663.2:g.155294721G=	GRCh38
NC_000001.10:g.155264512G= , CM000663.1:g.155264512G=	GRCh37
NC_000001.9:g.153531136G=	NCBI36
NG_011677.1:g.11714C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.726C= MANE Select	ENSP00000339933.4:p.Asn242=
ENST00000342741.4:c.726C=	ENSP00000339933.4:p.Asn242=
ENST00000392414.7:c.633C=	ENSP00000376214.3:p.Asn211=
NM_000298.5:c.726C=	NP_000289.1:p.Asn242=
NM_181871.3:c.633C=	NP_870986.1:p.Asn211=
XM_005245266.3:c.885C=	XP_005245323.1:p.Asn295=
XM_006711386.2:c.534C=	XP_006711449.1:p.Asn178=
XM_011509639.1:c.885C=	XP_011507941.1:p.Asn295=
XM_011509640.1:c.534C=	XP_011507942.1:p.Asn178=
NM_000298.6:c.726C= MANE Select	NP_000289.1:p.Asn242=
XM_006711386.4:c.534C=	XP_006711449.1:p.Asn178=
XM_011509640.3:c.534C=	XP_011507942.1:p.Asn178=
XM_017001493.1:c.726C=	XP_016856982.1:p.Asn242=
NM_181871.4:c.633C=	NP_870986.1:p.Asn211=