Canonical Allele Identifier: CA30903364

Gene: PKLR

Linked Data

• dbSNP Id: rs769783555
• MyVariant Identifiers: chr1:g.155264444G>C (hg19) ; chr1:g.155294653G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294653G>C , CM000663.2:g.155294653G>C	GRCh38
NC_000001.10:g.155264444G>C , CM000663.1:g.155264444G>C	GRCh37
NC_000001.9:g.153531068G>C	NCBI36
NG_011677.1:g.11782C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.794C>G MANE Select	ENSP00000339933.4:p.Ser265Cys
ENST00000342741.4:c.794C>G	ENSP00000339933.4:p.Ser265Cys
ENST00000392414.7:c.701C>G	ENSP00000376214.3:p.Ser234Cys
NM_000298.5:c.794C>G	NP_000289.1:p.Ser265Cys
NM_181871.3:c.701C>G	NP_870986.1:p.Ser234Cys
XM_005245266.3:c.953C>G	XP_005245323.1:p.Ser318Cys
XM_006711386.2:c.602C>G	XP_006711449.1:p.Ser201Cys
XM_011509639.1:c.953C>G	XP_011507941.1:p.Ser318Cys
XM_011509640.1:c.602C>G	XP_011507942.1:p.Ser201Cys
NM_000298.6:c.794C>G MANE Select	NP_000289.1:p.Ser265Cys
XM_006711386.4:c.602C>G	XP_006711449.1:p.Ser201Cys
XM_011509640.3:c.602C>G	XP_011507942.1:p.Ser201Cys
XM_017001493.1:c.794C>G	XP_016856982.1:p.Ser265Cys
NM_181871.4:c.701C>G	NP_870986.1:p.Ser234Cys