Canonical Allele Identifier: CA421245556

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155264341A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294550A>C , CM000663.2:g.155294550A>C	GRCh38
NC_000001.10:g.155264341A>C , CM000663.1:g.155264341A>C	GRCh37
NC_000001.9:g.153530965A>C	NCBI36
NG_011677.1:g.11885T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.897T>G MANE Select	ENSP00000339933.4:p.Ala299=
ENST00000342741.4:c.897T>G	ENSP00000339933.4:p.Ala299=
ENST00000392414.7:c.804T>G	ENSP00000376214.3:p.Ala268=
NM_000298.5:c.897T>G	NP_000289.1:p.Ala299=
NM_181871.3:c.804T>G	NP_870986.1:p.Ala268=
XM_005245266.3:c.1056T>G	XP_005245323.1:p.Ala352=
XM_006711386.2:c.705T>G	XP_006711449.1:p.Ala235=
XM_011509639.1:c.1056T>G	XP_011507941.1:p.Ala352=
XM_011509640.1:c.705T>G	XP_011507942.1:p.Ala235=
NM_000298.6:c.897T>G MANE Select	NP_000289.1:p.Ala299=
XM_006711386.4:c.705T>G	XP_006711449.1:p.Ala235=
XM_011509640.3:c.705T>G	XP_011507942.1:p.Ala235=
XM_017001493.1:c.897T>G	XP_016856982.1:p.Ala299=
NM_181871.4:c.804T>G	NP_870986.1:p.Ala268=