Canonical Allele Identifier: CA174864331

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31088900G>A , CM000670.2:g.31088900G>A	GRCh38
NC_000008.10:g.30946416G>A , CM000670.1:g.30946416G>A	GRCh37
NC_000008.9:g.31065958G>A	NCBI36
NG_008870.1:g.60639G>A , LRG_524:g.60639G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.1587G>A MANE Select	NP_000544.2:p.Trp529Ter
ENST00000298139.7:c.1587G>A MANE Select	ENSP00000298139.5:p.Trp529Ter
NM_000553.4:c.1587G>A , LRG_524t1:c.1587G>A	NP_000544.2:p.Trp529Ter
NM_000553.5:c.1587G>A	NP_000544.2:p.Trp529Ter
ENST00000298139.5:c.1587G>A	ENSP00000298139.5:p.Trp529Ter
ENST00000521620.5:n.288G>A
ENST00000650667.1:c.*1201G>A	ENSP00000498593.1:n.*1201G>A
XM_011544639.1:c.1506G>A	XP_011542941.1:p.Trp502Ter
XM_011544639.3:c.1506G>A	XP_011542941.1:p.Trp502Ter
XM_011544640.1:c.56G>A	XP_011542942.1:p.Gly19Asp
XM_024447265.1:c.1377G>A	XP_024303033.1:p.Trp459Ter
XR_949470.1:n.1860G>A
XR_949470.3:n.1888G>A
XR_949471.1:n.1860G>A
XR_949471.3:n.1888G>A
XR_949472.1:n.1860G>A
XR_949472.3:n.1888G>A