Canonical Allele Identifier: CA342748586

Gene: PKLR

Linked Data

• gnomAD v4: 1-155290660-A-T
• MyVariant Identifiers: chr1:g.155260451A>T (hg19) ; chr1:g.155290660A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155290660A>T , CM000663.2:g.155290660A>T	GRCh38
NC_000001.10:g.155260451A>T , CM000663.1:g.155260451A>T	GRCh37
NC_000001.9:g.153527075A>T	NCBI36
NG_011677.1:g.15775T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.1637T>A MANE Select	ENSP00000339933.4:p.Leu546His
ENST00000342741.4:c.1637T>A	ENSP00000339933.4:p.Leu546His
ENST00000392414.7:c.1544T>A	ENSP00000376214.3:p.Leu515His
NM_000298.5:c.1637T>A	NP_000289.1:p.Leu546His
NM_181871.3:c.1544T>A	NP_870986.1:p.Leu515His
XM_005245266.3:c.1796T>A	XP_005245323.1:p.Leu599His
XM_006711386.2:c.1445T>A	XP_006711449.1:p.Leu482His
XM_011509640.1:c.1445T>A	XP_011507942.1:p.Leu482His
NM_000298.6:c.1637T>A MANE Select	NP_000289.1:p.Leu546His
XM_006711386.4:c.1445T>A	XP_006711449.1:p.Leu482His
XM_011509640.3:c.1445T>A	XP_011507942.1:p.Leu482His
NM_181871.4:c.1544T>A	NP_870986.1:p.Leu515His