Canonical Allele Identifier: CA342751088

Gene: PKLR

Linked Data

• gnomAD v4: 1-155291855-G-A
• MyVariant Identifiers: chr1:g.155261646G>A (hg19) ; chr1:g.155291855G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155291855G>A , CM000663.2:g.155291855G>A	GRCh38
NC_000001.10:g.155261646G>A , CM000663.1:g.155261646G>A	GRCh37
NC_000001.9:g.153528270G>A	NCBI36
NG_011677.1:g.14580C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.1519C>T MANE Select	ENSP00000339933.4:p.His507Tyr
ENST00000342741.4:c.1519C>T	ENSP00000339933.4:p.His507Tyr
ENST00000392414.7:c.1426C>T	ENSP00000376214.3:p.His476Tyr
NM_000298.5:c.1519C>T	NP_000289.1:p.His507Tyr
NM_181871.3:c.1426C>T	NP_870986.1:p.His476Tyr
XM_005245266.3:c.1678C>T	XP_005245323.1:p.His560Tyr
XM_006711386.2:c.1327C>T	XP_006711449.1:p.His443Tyr
XM_011509640.1:c.1327C>T	XP_011507942.1:p.His443Tyr
NM_000298.6:c.1519C>T MANE Select	NP_000289.1:p.His507Tyr
XM_006711386.4:c.1327C>T	XP_006711449.1:p.His443Tyr
XM_011509640.3:c.1327C>T	XP_011507942.1:p.His443Tyr
NM_181871.4:c.1426C>T	NP_870986.1:p.His476Tyr