Canonical Allele Identifier: CA850754774

Gene: WRN

Linked Data

• dbSNP Id: rs1288555782
• gnomAD v4: 8-31173126-T-C
• MyVariant Identifiers: chr8:g.31030642T>C (hg19) ; chr8:g.31173126T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173126T>C , CM000670.2:g.31173126T>C	GRCh38
NC_000008.10:g.31030642T>C , CM000670.1:g.31030642T>C	GRCh37
NC_000008.9:g.31150184T>C	NCBI36
NG_008870.1:g.144865T>C , LRG_524:g.144865T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.*24T>C MANE Select	ENSP00000298139.5:n.*24T>C
ENST00000650667.1:c.*3937T>C	ENSP00000498593.1:n.*3937T>C
ENST00000651946.1:n.547T>C
ENST00000298139.5:c.*24T>C	ENSP00000298139.5:n.*24T>C
ENST00000521620.5:n.2956T>C
NM_000553.4:c.*24T>C , LRG_524t1:c.*24T>C	NP_000544.2:n.*24T>C
XM_011544639.1:c.*24T>C	XP_011542941.1:n.*24T>C
XM_011544640.1:c.*24T>C	XP_011542942.1:n.*24T>C
XR_949643.1:n.88-1808A>G
XR_949644.1:n.88-1808A>G
XR_949645.1:n.88-1808A>G
XR_949646.1:n.88-1808A>G
XR_949647.1:n.701-1808A>G
XR_949648.1:n.603-1808A>G
NM_000553.5:c.*24T>C	NP_000544.2:n.*24T>C
XM_011544639.3:c.*24T>C	XP_011542941.1:n.*24T>C
XM_024447265.1:c.*24T>C	XP_024303033.1:n.*24T>C
NM_000553.6:c.*24T>C MANE Select	NP_000544.2:n.*24T>C