Canonical Allele Identifier: CA370909521

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31167141G>A , CM000670.2:g.31167141G>A	GRCh38
NC_000008.10:g.31024657G>A , CM000670.1:g.31024657G>A	GRCh37
NC_000008.9:g.31144199G>A	NCBI36
NG_008870.1:g.138880G>A , LRG_524:g.138880G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.4102G>A MANE Select	NP_000544.2:p.Asp1368Asn
ENST00000298139.7:c.4102G>A MANE Select	ENSP00000298139.5:p.Asp1368Asn
NM_000553.4:c.4102G>A , LRG_524t1:c.4102G>A	NP_000544.2:p.Asp1368Asn
NM_000553.5:c.4102G>A	NP_000544.2:p.Asp1368Asn
ENST00000298139.5:c.4102G>A	ENSP00000298139.5:p.Asp1368Asn
ENST00000521620.5:n.2735G>A
ENST00000650667.1:c.*3716G>A	ENSP00000498593.1:n.*3716G>A
ENST00000651946.1:n.326G>A
XM_011544639.1:c.4021G>A	XP_011542941.1:p.Asp1341Asn
XM_011544639.3:c.4021G>A	XP_011542941.1:p.Asp1341Asn
XM_011544640.1:c.2503G>A	XP_011542942.1:p.Asp835Asn
XM_024447265.1:c.3892G>A	XP_024303033.1:p.Asp1298Asn
XR_949643.1:n.317C>T
XR_949644.1:n.317C>T
XR_949645.1:n.317C>T
XR_949646.1:n.317C>T
XR_949647.1:n.930C>T
XR_949648.1:n.832C>T