Canonical Allele Identifier: CA370915746

Gene: WRN

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31120398G>A , CM000670.2:g.31120398G>A	GRCh38
NC_000008.10:g.30977914G>A , CM000670.1:g.30977914G>A	GRCh37
NC_000008.9:g.31097456G>A	NCBI36
NG_008870.1:g.92137G>A , LRG_524:g.92137G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.2604G>A MANE Select	ENSP00000298139.5:p.Trp868Ter
ENST00000650667.1:c.*2218G>A	ENSP00000498593.1:n.*2218G>A
ENST00000298139.5:c.2604G>A	ENSP00000298139.5:p.Trp868Ter
ENST00000520169.1:n.443G>A
ENST00000521620.5:n.1237G>A
NM_000553.4:c.2604G>A , LRG_524t1:c.2604G>A	NP_000544.2:p.Trp868Ter
XM_011544639.1:c.2523G>A	XP_011542941.1:p.Trp841Ter
XM_011544640.1:c.1005G>A	XP_011542942.1:p.Trp335Ter
XR_949470.1:n.2877G>A
XR_949471.1:n.2877G>A
XR_949472.1:n.2877G>A
NM_000553.5:c.2604G>A	NP_000544.2:p.Trp868Ter
XM_011544639.3:c.2523G>A	XP_011542941.1:p.Trp841Ter
XM_024447265.1:c.2394G>A	XP_024303033.1:p.Trp798Ter
XR_949470.3:n.2905G>A
XR_949471.3:n.2905G>A
XR_949472.3:n.2905G>A
NM_000553.6:c.2604G>A MANE Select	NP_000544.2:p.Trp868Ter