Canonical Allele Identifier: CA30904535

Gene: PKLR

Linked Data

• dbSNP Id: rs929087559
• MyVariant Identifiers: chr1:g.155265238A>G (hg19) ; chr1:g.155295447A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155295447A>G , CM000663.2:g.155295447A>G	GRCh38
NC_000001.10:g.155265238A>G , CM000663.1:g.155265238A>G	GRCh37
NC_000001.9:g.153531862A>G	NCBI36
NG_011677.1:g.10988T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.497T>C MANE Select	ENSP00000339933.4:p.Ile166Thr
ENST00000434082.3:c.305T>C	ENSP00000398037.3:p.Ile102Thr
ENST00000342741.4:c.497T>C	ENSP00000339933.4:p.Ile166Thr
ENST00000392414.7:c.404T>C	ENSP00000376214.3:p.Ile135Thr
ENST00000434082.2:c.402T>C	ENSP00000398037.2:n.402T>C
NM_000298.5:c.497T>C	NP_000289.1:p.Ile166Thr
NM_181871.3:c.404T>C	NP_870986.1:p.Ile135Thr
XM_005245266.3:c.656T>C	XP_005245323.1:p.Ile219Thr
XM_006711386.2:c.305T>C	XP_006711449.1:p.Ile102Thr
XM_011509639.1:c.656T>C	XP_011507941.1:p.Ile219Thr
XM_011509640.1:c.305T>C	XP_011507942.1:p.Ile102Thr
NM_000298.6:c.497T>C MANE Select	NP_000289.1:p.Ile166Thr
XM_006711386.4:c.305T>C	XP_006711449.1:p.Ile102Thr
XM_011509640.3:c.305T>C	XP_011507942.1:p.Ile102Thr
XM_017001493.1:c.497T>C	XP_016856982.1:p.Ile166Thr
NM_181871.4:c.404T>C	NP_870986.1:p.Ile135Thr