Canonical Allele Identifier: CA10607957

Gene: PKLR

Linked Data

• ClinVar Variation Id: 292801
• ClinVar RCV Id: RCV000338287
• dbSNP Id: rs886045350
• gnomAD v3: 1-155290297-G-A
• gnomAD v4: 1-155290297-G-A
• MyVariant Identifiers: chr1:g.155260088G>A (hg19) ; chr1:g.155290297G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155290297G>A , CM000663.2:g.155290297G>A	GRCh38
NC_000001.10:g.155260088G>A , CM000663.1:g.155260088G>A	GRCh37
NC_000001.9:g.153526712G>A	NCBI36
NG_011677.1:g.16138C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.*275C>T MANE Select	ENSP00000339933.4:n.*275C>T
ENST00000342741.4:c.*275C>T	ENSP00000339933.4:n.*275C>T
ENST00000392414.7:c.*275C>T	ENSP00000376214.3:n.*275C>T
NM_000298.5:c.*275C>T	NP_000289.1:n.*275C>T
NM_181871.3:c.*275C>T	NP_870986.1:n.*275C>T
XM_005245266.3:c.*275C>T	XP_005245323.1:n.*275C>T
XM_006711386.2:c.*275C>T	XP_006711449.1:n.*275C>T
XM_011509640.1:c.*275C>T	XP_011507942.1:n.*275C>T
NM_000298.6:c.*275C>T MANE Select	NP_000289.1:n.*275C>T
XM_006711386.4:c.*275C>T	XP_006711449.1:n.*275C>T
XM_011509640.3:c.*275C>T	XP_011507942.1:n.*275C>T
NM_181871.4:c.*275C>T	NP_870986.1:n.*275C>T