Canonical Allele Identifier: CA421020447

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155264524G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294733G>T , CM000663.2:g.155294733G>T	GRCh38
NC_000001.10:g.155264524G>T , CM000663.1:g.155264524G>T	GRCh37
NC_000001.9:g.153531148G>T	NCBI36
NG_011677.1:g.11702C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.714C>A MANE Select	ENSP00000339933.4:p.Thr238=
ENST00000342741.4:c.714C>A	ENSP00000339933.4:p.Thr238=
ENST00000392414.7:c.621C>A	ENSP00000376214.3:p.Thr207=
NM_000298.5:c.714C>A	NP_000289.1:p.Thr238=
NM_181871.3:c.621C>A	NP_870986.1:p.Thr207=
XM_005245266.3:c.873C>A	XP_005245323.1:p.Thr291=
XM_006711386.2:c.522C>A	XP_006711449.1:p.Thr174=
XM_011509639.1:c.873C>A	XP_011507941.1:p.Thr291=
XM_011509640.1:c.522C>A	XP_011507942.1:p.Thr174=
NM_000298.6:c.714C>A MANE Select	NP_000289.1:p.Thr238=
XM_006711386.4:c.522C>A	XP_006711449.1:p.Thr174=
XM_011509640.3:c.522C>A	XP_011507942.1:p.Thr174=
XM_017001493.1:c.714C>A	XP_016856982.1:p.Thr238=
NM_181871.4:c.621C>A	NP_870986.1:p.Thr207=