Canonical Allele Identifier: CA370923634

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31085165G>A , CM000670.2:g.31085165G>A	GRCh38
NC_000008.10:g.30942681G>A , CM000670.1:g.30942681G>A	GRCh37
NC_000008.9:g.31062223G>A	NCBI36
NG_008870.1:g.56904G>A , LRG_524:g.56904G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.1351-1G>A MANE Select	NP_000544.2:n.1351-1G>A
ENST00000298139.7:c.1351-1G>A MANE Select	ENSP00000298139.5:n.1351-1G>A
NM_000553.4:c.1351-1G>A , LRG_524t1:c.1351-1G>A	NP_000544.2:n.1351-1G>A
NM_000553.5:c.1351-1G>A	NP_000544.2:n.1351-1G>A
ENST00000298139.5:c.1351-1G>A	ENSP00000298139.5:n.1351-1G>A
ENST00000650667.1:c.*965-1G>A	ENSP00000498593.1:n.*965-1G>A
ENST00000651642.1:c.565-1G>A	ENSP00000498779.1:n.565-1G>A
XM_011544639.1:c.1350+1386G>A	XP_011542941.1:n.1350+1386G>A
XM_011544639.3:c.1350+1386G>A	XP_011542941.1:n.1350+1386G>A
XM_024447265.1:c.1141-1G>A	XP_024303033.1:n.1141-1G>A
XR_949470.1:n.1624-1G>A
XR_949470.3:n.1652-1G>A
XR_949471.1:n.1624-1G>A
XR_949471.3:n.1652-1G>A
XR_949472.1:n.1624-1G>A
XR_949472.3:n.1652-1G>A