Canonical Allele Identifier: CA460228398

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.31030555C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173039C>A , CM000670.2:g.31173039C>A	GRCh38
NC_000008.10:g.31030555C>A , CM000670.1:g.31030555C>A	GRCh37
NC_000008.9:g.31150097C>A	NCBI36
NG_008870.1:g.144778C>A , LRG_524:g.144778C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.4236C>A MANE Select	ENSP00000298139.5:p.Ala1412=
ENST00000650667.1:c.*3850C>A	ENSP00000498593.1:n.*3850C>A
ENST00000651946.1:n.460C>A
ENST00000298139.5:c.4236C>A	ENSP00000298139.5:p.Ala1412=
ENST00000521620.5:n.2869C>A
NM_000553.4:c.4236C>A , LRG_524t1:c.4236C>A	NP_000544.2:p.Ala1412=
XM_011544639.1:c.4155C>A	XP_011542941.1:p.Ala1385=
XM_011544640.1:c.2637C>A	XP_011542942.1:p.Ala879=
XR_949643.1:n.88-1721G>T
XR_949644.1:n.88-1721G>T
XR_949645.1:n.88-1721G>T
XR_949646.1:n.88-1721G>T
XR_949647.1:n.701-1721G>T
XR_949648.1:n.603-1721G>T
NM_000553.5:c.4236C>A	NP_000544.2:p.Ala1412=
XM_011544639.3:c.4155C>A	XP_011542941.1:p.Ala1385=
XM_024447265.1:c.4026C>A	XP_024303033.1:p.Ala1342=
NM_000553.6:c.4236C>A MANE Select	NP_000544.2:p.Ala1412=