Canonical Allele Identifier: CA370912280

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31058535G>T , CM000670.2:g.31058535G>T	GRCh38
NC_000008.10:g.30916051G>T , CM000670.1:g.30916051G>T	GRCh37
NC_000008.9:g.31035593G>T	NCBI36
NG_008870.1:g.30274G>T , LRG_524:g.30274G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.88G>T MANE Select	NP_000544.2:p.Glu30Ter
ENST00000298139.7:c.88G>T MANE Select	ENSP00000298139.5:p.Glu30Ter
NM_000553.4:c.88G>T , LRG_524t1:c.88G>T	NP_000544.2:p.Glu30Ter
NM_000553.5:c.88G>T	NP_000544.2:p.Glu30Ter
ENST00000298139.5:c.88G>T	ENSP00000298139.5:p.Glu30Ter
ENST00000650667.1:c.88G>T	ENSP00000498593.1:p.Glu30Ter
XM_011544639.1:c.88G>T	XP_011542941.1:p.Glu30Ter
XM_011544639.3:c.88G>T	XP_011542941.1:p.Glu30Ter
XM_024447265.1:c.-247G>T	XP_024303033.1:n.-247G>T
XR_949470.1:n.361G>T
XR_949470.3:n.389G>T
XR_949471.1:n.361G>T
XR_949471.3:n.389G>T
XR_949472.1:n.361G>T
XR_949472.3:n.389G>T