Canonical Allele Identifier: CA253493

Gene: WRN

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31090843A>T , CM000670.2:g.31090843A>T	GRCh38
NC_000008.10:g.30948359A>T , CM000670.1:g.30948359A>T	GRCh37
NC_000008.9:g.31067901A>T	NCBI36
NG_008870.1:g.62582A>T , LRG_524:g.62582A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.1730A>T MANE Select	ENSP00000298139.5:p.Lys577Met
ENST00000650667.1:c.*1344A>T	ENSP00000498593.1:n.*1344A>T
ENST00000298139.5:c.1730A>T	ENSP00000298139.5:p.Lys577Met
ENST00000521620.5:n.363A>T
NM_000553.4:c.1730A>T , LRG_524t1:c.1730A>T	NP_000544.2:p.Lys577Met
XM_011544639.1:c.1649A>T	XP_011542941.1:p.Lys550Met
XM_011544640.1:c.131A>T	XP_011542942.1:p.Lys44Met
XR_949470.1:n.2003A>T
XR_949471.1:n.2003A>T
XR_949472.1:n.2003A>T
NM_000553.5:c.1730A>T	NP_000544.2:p.Lys577Met
XM_011544639.3:c.1649A>T	XP_011542941.1:p.Lys550Met
XM_024447265.1:c.1520A>T	XP_024303033.1:p.Lys507Met
XR_949470.3:n.2031A>T
XR_949471.3:n.2031A>T
XR_949472.3:n.2031A>T
NM_000553.6:c.1730A>T MANE Select	NP_000544.2:p.Lys577Met