Canonical Allele Identifier: CA2686834251

Gene: WRN

Linked Data

• gnomAD v4: 8-31033969-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033969T>C , CM000670.2:g.31033969T>C	GRCh38
NC_000008.10:g.30891485T>C , CM000670.1:g.30891485T>C	GRCh37
NC_000008.9:g.31011027T>C	NCBI36
NG_008870.1:g.5708T>C , LRG_524:g.5708T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.-81T>C MANE Select	ENSP00000298139.5:n.-81T>C
ENST00000650667.1:c.-81T>C	ENSP00000498593.1:n.-81T>C
ENST00000298139.5:c.-81T>C	ENSP00000298139.5:n.-81T>C
NM_000553.4:c.-81T>C , LRG_524t1:c.-81T>C	NP_000544.2:n.-81T>C
XM_011544639.1:c.-81T>C	XP_011542941.1:n.-81T>C
XR_949470.1:n.193T>C
XR_949471.1:n.193T>C
XR_949472.1:n.193T>C
NM_000553.5:c.-81T>C	NP_000544.2:n.-81T>C
XM_011544639.3:c.-81T>C	XP_011542941.1:n.-81T>C
XM_024447265.1:c.-415T>C	XP_024303033.1:n.-415T>C
XR_949470.3:n.221T>C
XR_949471.3:n.221T>C
XR_949472.3:n.221T>C
NM_000553.6:c.-81T>C MANE Select	NP_000544.2:n.-81T>C