Canonical Allele Identifier: CA342758473

Gene: PKLR

Linked Data

• MyVariant Identifiers: chr1:g.155269984G>T (hg19) ; chr1:g.155300193G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155300193G>T , CM000663.2:g.155300193G>T	GRCh38
NC_000001.10:g.155269984G>T , CM000663.1:g.155269984G>T	GRCh37
NC_000001.9:g.153536608G>T	NCBI36
NG_011677.1:g.6242C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.188C>A MANE Select	ENSP00000339933.4:p.Ala63Asp
ENST00000434082.3:c.-5C>A	ENSP00000398037.3:n.-5C>A
ENST00000342741.4:c.188C>A	ENSP00000339933.4:p.Ala63Asp
ENST00000392414.7:c.95C>A	ENSP00000376214.3:p.Ala32Asp
ENST00000434082.2:c.93C>A	ENSP00000398037.2:p.Ser31Arg
NM_000298.5:c.188C>A	NP_000289.1:p.Ala63Asp
NM_181871.3:c.95C>A	NP_870986.1:p.Ala32Asp
XM_005245266.3:c.347C>A	XP_005245323.1:p.Ala116Asp
XM_006711386.2:c.-5C>A	XP_006711449.1:n.-5C>A
XM_011509639.1:c.347C>A	XP_011507941.1:p.Ala116Asp
XM_011509640.1:c.-5C>A	XP_011507942.1:n.-5C>A
NM_000298.6:c.188C>A MANE Select	NP_000289.1:p.Ala63Asp
XM_006711386.4:c.-5C>A	XP_006711449.1:n.-5C>A
XM_011509640.3:c.-5C>A	XP_011507942.1:n.-5C>A
XM_017001493.1:c.188C>A	XP_016856982.1:p.Ala63Asp
NM_181871.4:c.95C>A	NP_870986.1:p.Ala32Asp