Canonical Allele Identifier: CA2686834157

Gene: WRN

Linked Data

• gnomAD v4: 8-31033838-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033838G>T , CM000670.2:g.31033838G>T	GRCh38
NC_000008.10:g.30891354G>T , CM000670.1:g.30891354G>T	GRCh37
NC_000008.9:g.31010896G>T	NCBI36
NG_008870.1:g.5577G>T , LRG_524:g.5577G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.-212G>T MANE Select	ENSP00000298139.5:n.-212G>T
ENST00000650667.1:c.-212G>T	ENSP00000498593.1:n.-212G>T
ENST00000298139.5:c.-212G>T	ENSP00000298139.5:n.-212G>T
NM_000553.4:c.-212G>T , LRG_524t1:c.-212G>T	NP_000544.2:n.-212G>T
XM_011544639.1:c.-212G>T	XP_011542941.1:n.-212G>T
XR_949470.1:n.62G>T
XR_949471.1:n.62G>T
XR_949472.1:n.62G>T
NM_000553.5:c.-212G>T	NP_000544.2:n.-212G>T
XM_011544639.3:c.-212G>T	XP_011542941.1:n.-212G>T
XM_024447265.1:c.-546G>T	XP_024303033.1:n.-546G>T
XR_949470.3:n.90G>T
XR_949471.3:n.90G>T
XR_949472.3:n.90G>T
NM_000553.6:c.-212G>T MANE Select	NP_000544.2:n.-212G>T