Canonical Allele Identifier: CA342753861

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155264316T>C (hg19) ; chr1:g.155294525T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294525T>C , CM000663.2:g.155294525T>C	GRCh38
NC_000001.10:g.155264316T>C , CM000663.1:g.155264316T>C	GRCh37
NC_000001.9:g.153530940T>C	NCBI36
NG_011677.1:g.11910A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.922A>G MANE Select	ENSP00000339933.4:p.Ile308Val
ENST00000342741.4:c.922A>G	ENSP00000339933.4:p.Ile308Val
ENST00000392414.7:c.829A>G	ENSP00000376214.3:p.Ile277Val
NM_000298.5:c.922A>G	NP_000289.1:p.Ile308Val
NM_181871.3:c.829A>G	NP_870986.1:p.Ile277Val
XM_005245266.3:c.1081A>G	XP_005245323.1:p.Ile361Val
XM_006711386.2:c.730A>G	XP_006711449.1:p.Ile244Val
XM_011509639.1:c.1081A>G	XP_011507941.1:p.Ile361Val
XM_011509640.1:c.730A>G	XP_011507942.1:p.Ile244Val
NM_000298.6:c.922A>G MANE Select	NP_000289.1:p.Ile308Val
XM_006711386.4:c.730A>G	XP_006711449.1:p.Ile244Val
XM_011509640.3:c.730A>G	XP_011507942.1:p.Ile244Val
XM_017001493.1:c.922A>G	XP_016856982.1:p.Ile308Val
NM_181871.4:c.829A>G	NP_870986.1:p.Ile277Val