Canonical Allele Identifier: CA1143963

Gene: PKLR

Linked Data

• ClinVar Variation Id: 1324921
• ClinVar RCV Id: RCV001782641
• dbSNP Id: rs758278200
• ExAC: 1:155261570 C / T
• gnomAD v2: 1-155261570-C-T
• gnomAD v4: 1-155291779-C-T
• MyVariant Identifiers: chr1:g.155261570C>T (hg19) ; chr1:g.155291779C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155291779C>T , CM000663.2:g.155291779C>T	GRCh38
NC_000001.10:g.155261570C>T , CM000663.1:g.155261570C>T	GRCh37
NC_000001.9:g.153528194C>T	NCBI36
NG_011677.1:g.14656G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342741.6:c.1595G>A MANE Select	ENSP00000339933.4:p.Arg532Gln
ENST00000342741.4:c.1595G>A	ENSP00000339933.4:p.Arg532Gln
ENST00000392414.7:c.1502G>A	ENSP00000376214.3:p.Arg501Gln
NM_000298.5:c.1595G>A	NP_000289.1:p.Arg532Gln
NM_181871.3:c.1502G>A	NP_870986.1:p.Arg501Gln
XM_005245266.3:c.1754G>A	XP_005245323.1:p.Arg585Gln
XM_006711386.2:c.1403G>A	XP_006711449.1:p.Arg468Gln
XM_011509640.1:c.1403G>A	XP_011507942.1:p.Arg468Gln
NM_000298.6:c.1595G>A MANE Select	NP_000289.1:p.Arg532Gln
XM_006711386.4:c.1403G>A	XP_006711449.1:p.Arg468Gln
XM_011509640.3:c.1403G>A	XP_011507942.1:p.Arg468Gln
NM_181871.4:c.1502G>A	NP_870986.1:p.Arg501Gln