Canonical Allele Identifier: CA370909615

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31167150A>T , CM000670.2:g.31167150A>T	GRCh38
NC_000008.10:g.31024666A>T , CM000670.1:g.31024666A>T	GRCh37
NC_000008.9:g.31144208A>T	NCBI36
NG_008870.1:g.138889A>T , LRG_524:g.138889A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.4111A>T MANE Select	NP_000544.2:p.Lys1371Ter
ENST00000298139.7:c.4111A>T MANE Select	ENSP00000298139.5:p.Lys1371Ter
NM_000553.4:c.4111A>T , LRG_524t1:c.4111A>T	NP_000544.2:p.Lys1371Ter
NM_000553.5:c.4111A>T	NP_000544.2:p.Lys1371Ter
ENST00000298139.5:c.4111A>T	ENSP00000298139.5:p.Lys1371Ter
ENST00000521620.5:n.2744A>T
ENST00000650667.1:c.*3725A>T	ENSP00000498593.1:n.*3725A>T
ENST00000651946.1:n.335A>T
XM_011544639.1:c.4030A>T	XP_011542941.1:p.Lys1344Ter
XM_011544639.3:c.4030A>T	XP_011542941.1:p.Lys1344Ter
XM_011544640.1:c.2512A>T	XP_011542942.1:p.Lys838Ter
XM_024447265.1:c.3901A>T	XP_024303033.1:p.Lys1301Ter
XR_949643.1:n.308T>A
XR_949644.1:n.308T>A
XR_949645.1:n.308T>A
XR_949646.1:n.308T>A
XR_949647.1:n.921T>A
XR_949648.1:n.823T>A