Canonical Allele Identifier: CA2686834172

Gene: WRN

Linked Data

• gnomAD v4: 8-31033861-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033861T>C , CM000670.2:g.31033861T>C	GRCh38
NC_000008.10:g.30891377T>C , CM000670.1:g.30891377T>C	GRCh37
NC_000008.9:g.31010919T>C	NCBI36
NG_008870.1:g.5600T>C , LRG_524:g.5600T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.-189T>C MANE Select	ENSP00000298139.5:n.-189T>C
ENST00000650667.1:c.-189T>C	ENSP00000498593.1:n.-189T>C
ENST00000298139.5:c.-189T>C	ENSP00000298139.5:n.-189T>C
NM_000553.4:c.-189T>C , LRG_524t1:c.-189T>C	NP_000544.2:n.-189T>C
XM_011544639.1:c.-189T>C	XP_011542941.1:n.-189T>C
XR_949470.1:n.85T>C
XR_949471.1:n.85T>C
XR_949472.1:n.85T>C
NM_000553.5:c.-189T>C	NP_000544.2:n.-189T>C
XM_011544639.3:c.-189T>C	XP_011542941.1:n.-189T>C
XM_024447265.1:c.-523T>C	XP_024303033.1:n.-523T>C
XR_949470.3:n.113T>C
XR_949471.3:n.113T>C
XR_949472.3:n.113T>C
NM_000553.6:c.-189T>C MANE Select	NP_000544.2:n.-189T>C