Canonical Allele Identifier: CA4705235

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31167021G>T , CM000670.2:g.31167021G>T	GRCh38
NC_000008.10:g.31024537G>T , CM000670.1:g.31024537G>T	GRCh37
NC_000008.9:g.31144079G>T	NCBI36
NG_008870.1:g.138760G>T , LRG_524:g.138760G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.3983-1G>T MANE Select	NP_000544.2:n.3983-1G>T
ENST00000298139.7:c.3983-1G>T MANE Select	ENSP00000298139.5:n.3983-1G>T
NM_000553.4:c.3983-1G>T , LRG_524t1:c.3983-1G>T	NP_000544.2:n.3983-1G>T
NM_000553.5:c.3983-1G>T	NP_000544.2:n.3983-1G>T
ENST00000298139.5:c.3983-1G>T	ENSP00000298139.5:n.3983-1G>T
ENST00000521620.5:n.2616-1G>T
ENST00000650667.1:c.*3597-1G>T	ENSP00000498593.1:n.*3597-1G>T
ENST00000651946.1:n.207-1G>T
XM_011544639.1:c.3902-1G>T	XP_011542941.1:n.3902-1G>T
XM_011544639.3:c.3902-1G>T	XP_011542941.1:n.3902-1G>T
XM_011544640.1:c.2384-1G>T	XP_011542942.1:n.2384-1G>T
XM_024447265.1:c.3773-1G>T	XP_024303033.1:n.3773-1G>T
XR_949470.1:n.4347-1G>T
XR_949470.3:n.4375-1G>T
XR_949471.1:n.4710-1G>T
XR_949471.3:n.4738-1G>T
XR_949472.1:n.4619-1G>T
XR_949472.3:n.4647-1G>T
XR_949643.1:n.380+57C>A
XR_949644.1:n.380+57C>A
XR_949645.1:n.380+57C>A
XR_949646.1:n.380+57C>A
XR_949647.1:n.993+57C>A
XR_949648.1:n.895+57C>A