Canonical Allele Identifier: CA342755420

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155265226A>C (hg19) ; chr1:g.155295435A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155295435A>C , CM000663.2:g.155295435A>C	GRCh38
NC_000001.10:g.155265226A>C , CM000663.1:g.155265226A>C	GRCh37
NC_000001.9:g.153531850A>C	NCBI36
NG_011677.1:g.11000T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.507+2T>G MANE Select	ENSP00000339933.4:n.507+2T>G
ENST00000434082.3:c.315+2T>G	ENSP00000398037.3:n.315+2T>G
ENST00000342741.4:c.507+2T>G	ENSP00000339933.4:n.507+2T>G
ENST00000392414.7:c.414+2T>G	ENSP00000376214.3:n.414+2T>G
ENST00000434082.2:c.412+2T>G	ENSP00000398037.2:n.412+2T>G
NM_000298.5:c.507+2T>G	NP_000289.1:n.507+2T>G
NM_181871.3:c.414+2T>G	NP_870986.1:n.414+2T>G
XM_005245266.3:c.666+2T>G	XP_005245323.1:n.666+2T>G
XM_006711386.2:c.315+2T>G	XP_006711449.1:n.315+2T>G
XM_011509639.1:c.666+2T>G	XP_011507941.1:n.666+2T>G
XM_011509640.1:c.315+2T>G	XP_011507942.1:n.315+2T>G
NM_000298.6:c.507+2T>G MANE Select	NP_000289.1:n.507+2T>G
XM_006711386.4:c.315+2T>G	XP_006711449.1:n.315+2T>G
XM_011509640.3:c.315+2T>G	XP_011507942.1:n.315+2T>G
XM_017001493.1:c.507+2T>G	XP_016856982.1:n.507+2T>G
NM_181871.4:c.414+2T>G	NP_870986.1:n.414+2T>G