Canonical Allele Identifier: CA10608322

Gene: PKLR

Linked Data

• ClinVar Variation Id: 292802
• ClinVar RCV Id: RCV001689967
• dbSNP Id: rs932972
• gnomAD v2: 1-155260096-G-A
• gnomAD v3: 1-155290305-G-A
• gnomAD v4: 1-155290305-G-A
• MyVariant Identifiers: chr1:g.155260096G>A (hg19) ; chr1:g.155290305G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155290305G>A , CM000663.2:g.155290305G>A	GRCh38
NC_000001.10:g.155260096G>A , CM000663.1:g.155260096G>A	GRCh37
NC_000001.9:g.153526720G>A	NCBI36
NG_011677.1:g.16130C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342741.6:c.*267C>T MANE Select	ENSP00000339933.4:n.*267C>T
ENST00000342741.4:c.*267C>T	ENSP00000339933.4:n.*267C>T
ENST00000392414.7:c.*267C>T	ENSP00000376214.3:n.*267C>T
NM_000298.5:c.*267C>T	NP_000289.1:n.*267C>T
NM_181871.3:c.*267C>T	NP_870986.1:n.*267C>T
XM_005245266.3:c.*267C>T	XP_005245323.1:n.*267C>T
XM_006711386.2:c.*267C>T	XP_006711449.1:n.*267C>T
XM_011509640.1:c.*267C>T	XP_011507942.1:n.*267C>T
NM_000298.6:c.*267C>T MANE Select	NP_000289.1:n.*267C>T
XM_006711386.4:c.*267C>T	XP_006711449.1:n.*267C>T
XM_011509640.3:c.*267C>T	XP_011507942.1:n.*267C>T
NM_181871.4:c.*267C>T	NP_870986.1:n.*267C>T