Canonical Allele Identifier: CA370913613

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31116430C>T , CM000670.2:g.31116430C>T	GRCh38
NC_000008.10:g.30973946C>T , CM000670.1:g.30973946C>T	GRCh37
NC_000008.9:g.31093488C>T	NCBI36
NG_008870.1:g.88169C>T , LRG_524:g.88169C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.2350C>T MANE Select	NP_000544.2:p.Leu784Phe
ENST00000298139.7:c.2350C>T MANE Select	ENSP00000298139.5:p.Leu784Phe
NM_000553.4:c.2350C>T , LRG_524t1:c.2350C>T	NP_000544.2:p.Leu784Phe
NM_000553.5:c.2350C>T	NP_000544.2:p.Leu784Phe
ENST00000298139.5:c.2350C>T	ENSP00000298139.5:p.Leu784Phe
ENST00000521620.5:n.983C>T
ENST00000650667.1:c.*1964C>T	ENSP00000498593.1:n.*1964C>T
XM_011544639.1:c.2269C>T	XP_011542941.1:p.Leu757Phe
XM_011544639.3:c.2269C>T	XP_011542941.1:p.Leu757Phe
XM_011544640.1:c.751C>T	XP_011542942.1:p.Leu251Phe
XM_024447265.1:c.2140C>T	XP_024303033.1:p.Leu714Phe
XR_949470.1:n.2623C>T
XR_949470.3:n.2651C>T
XR_949471.1:n.2623C>T
XR_949471.3:n.2651C>T
XR_949472.1:n.2623C>T
XR_949472.3:n.2651C>T