Canonical Allele Identifier: CA2648266552

Gene: PKLR

Linked Data

• gnomAD v4: 1-155290336-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155290336G>A , CM000663.2:g.155290336G>A	GRCh38
NC_000001.10:g.155260127G>A , CM000663.1:g.155260127G>A	GRCh37
NC_000001.9:g.153526751G>A	NCBI36
NG_011677.1:g.16099C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.*236C>T MANE Select	ENSP00000339933.4:n.*236C>T
ENST00000342741.4:c.*236C>T	ENSP00000339933.4:n.*236C>T
ENST00000392414.7:c.*236C>T	ENSP00000376214.3:n.*236C>T
NM_000298.5:c.*236C>T	NP_000289.1:n.*236C>T
NM_181871.3:c.*236C>T	NP_870986.1:n.*236C>T
XM_005245266.3:c.*236C>T	XP_005245323.1:n.*236C>T
XM_006711386.2:c.*236C>T	XP_006711449.1:n.*236C>T
XM_011509640.1:c.*236C>T	XP_011507942.1:n.*236C>T
NM_000298.6:c.*236C>T MANE Select	NP_000289.1:n.*236C>T
XM_006711386.4:c.*236C>T	XP_006711449.1:n.*236C>T
XM_011509640.3:c.*236C>T	XP_011507942.1:n.*236C>T
NM_181871.4:c.*236C>T	NP_870986.1:n.*236C>T