Canonical Allele Identifier: CA2843388239

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033896del , CM000670.2:g.31033896del	GRCh38
NC_000008.10:g.30891412del , CM000670.1:g.30891412del	GRCh37
NC_000008.9:g.31010954del	NCBI36
NG_008870.1:g.5635del , LRG_524:g.5635del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.-154del MANE Select	ENSP00000298139.5:n.-154del
ENST00000650667.1:c.-154del	ENSP00000498593.1:n.-154del
ENST00000298139.5:c.-154del	ENSP00000298139.5:n.-154del
NM_000553.4:c.-154del , LRG_524t1:c.-154del	NP_000544.2:n.-154del
XM_011544639.1:c.-154del	XP_011542941.1:n.-154del
XR_949470.1:n.120del
XR_949471.1:n.120del
XR_949472.1:n.120del
NM_000553.5:c.-154del	NP_000544.2:n.-154del
XM_011544639.3:c.-154del	XP_011542941.1:n.-154del
XM_024447265.1:c.-488del	XP_024303033.1:n.-488del
XR_949470.3:n.148del
XR_949471.3:n.148del
XR_949472.3:n.148del
NM_000553.6:c.-154del MANE Select	NP_000544.2:n.-154del