Canonical Allele Identifier: CA370920162

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31081021C>T , CM000670.2:g.31081021C>T	GRCh38
NC_000008.10:g.30938537C>T , CM000670.1:g.30938537C>T	GRCh37
NC_000008.9:g.31058079C>T	NCBI36
NG_008870.1:g.52760C>T , LRG_524:g.52760C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.994C>T MANE Select	NP_000544.2:p.Gln332Ter
ENST00000298139.7:c.994C>T MANE Select	ENSP00000298139.5:p.Gln332Ter
NM_000553.4:c.994C>T , LRG_524t1:c.994C>T	NP_000544.2:p.Gln332Ter
NM_000553.5:c.994C>T	NP_000544.2:p.Gln332Ter
ENST00000298139.5:c.994C>T	ENSP00000298139.5:p.Gln332Ter
ENST00000650667.1:c.*608C>T	ENSP00000498593.1:n.*608C>T
ENST00000651642.1:c.289C>T	ENSP00000498779.1:p.Gln97Ter
XM_011544639.1:c.994C>T	XP_011542941.1:p.Gln332Ter
XM_011544639.3:c.994C>T	XP_011542941.1:p.Gln332Ter
XM_024447265.1:c.784C>T	XP_024303033.1:p.Gln262Ter
XR_949470.1:n.1267C>T
XR_949470.3:n.1295C>T
XR_949471.1:n.1267C>T
XR_949471.3:n.1295C>T
XR_949472.1:n.1267C>T
XR_949472.3:n.1295C>T