Canonical Allele Identifier: CA342753810

Gene: PKLR

Linked Data

• gnomAD v4: 1-155294515-A-G
• MyVariant Identifiers: chr1:g.155264306A>G (hg19) ; chr1:g.155294515A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294515A>G , CM000663.2:g.155294515A>G	GRCh38
NC_000001.10:g.155264306A>G , CM000663.1:g.155264306A>G	GRCh37
NC_000001.9:g.153530930A>G	NCBI36
NG_011677.1:g.11920T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.932T>C MANE Select	ENSP00000339933.4:p.Ile311Thr
ENST00000342741.4:c.932T>C	ENSP00000339933.4:p.Ile311Thr
ENST00000392414.7:c.839T>C	ENSP00000376214.3:p.Ile280Thr
NM_000298.5:c.932T>C	NP_000289.1:p.Ile311Thr
NM_181871.3:c.839T>C	NP_870986.1:p.Ile280Thr
XM_005245266.3:c.1091T>C	XP_005245323.1:p.Ile364Thr
XM_006711386.2:c.740T>C	XP_006711449.1:p.Ile247Thr
XM_011509639.1:c.1091T>C	XP_011507941.1:p.Ile364Thr
XM_011509640.1:c.740T>C	XP_011507942.1:p.Ile247Thr
NM_000298.6:c.932T>C MANE Select	NP_000289.1:p.Ile311Thr
XM_006711386.4:c.740T>C	XP_006711449.1:p.Ile247Thr
XM_011509640.3:c.740T>C	XP_011507942.1:p.Ile247Thr
XM_017001493.1:c.932T>C	XP_016856982.1:p.Ile311Thr
NM_181871.4:c.839T>C	NP_870986.1:p.Ile280Thr