Canonical Allele Identifier: CA342754726

Gene: PKLR

Linked Data

• gnomAD v4: 1-155294729-C-T
• MyVariant Identifiers: chr1:g.155264520C>T (hg19) ; chr1:g.155294729C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155294729C>T , CM000663.2:g.155294729C>T	GRCh38
NC_000001.10:g.155264520C>T , CM000663.1:g.155264520C>T	GRCh37
NC_000001.9:g.153531144C>T	NCBI36
NG_011677.1:g.11706G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342741.6:c.718G>A MANE Select	ENSP00000339933.4:p.Val240Met
ENST00000342741.4:c.718G>A	ENSP00000339933.4:p.Val240Met
ENST00000392414.7:c.625G>A	ENSP00000376214.3:p.Val209Met
NM_000298.5:c.718G>A	NP_000289.1:p.Val240Met
NM_181871.3:c.625G>A	NP_870986.1:p.Val209Met
XM_005245266.3:c.877G>A	XP_005245323.1:p.Val293Met
XM_006711386.2:c.526G>A	XP_006711449.1:p.Val176Met
XM_011509639.1:c.877G>A	XP_011507941.1:p.Val293Met
XM_011509640.1:c.526G>A	XP_011507942.1:p.Val176Met
NM_000298.6:c.718G>A MANE Select	NP_000289.1:p.Val240Met
XM_006711386.4:c.526G>A	XP_006711449.1:p.Val176Met
XM_011509640.3:c.526G>A	XP_011507942.1:p.Val176Met
XM_017001493.1:c.718G>A	XP_016856982.1:p.Val240Met
NM_181871.4:c.625G>A	NP_870986.1:p.Val209Met