Canonical Allele Identifier: CA2573049688

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31120201T= , CM000670.2:g.31120201T=	GRCh38
NC_000008.10:g.30977717T= , CM000670.1:g.30977717T=	GRCh37
NC_000008.9:g.31097259T=	NCBI36
NG_008870.1:g.91940T= , LRG_524:g.91940T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.2449-42T= MANE Select	ENSP00000298139.5:n.2449-42T=
ENST00000650667.1:c.*2063-42T=	ENSP00000498593.1:n.*2063-42T=
ENST00000298139.5:c.2449-42T=	ENSP00000298139.5:n.2449-42T=
ENST00000520169.1:n.246T=
ENST00000521620.5:n.1082-42T=
NM_000553.4:c.2449-42T= , LRG_524t1:c.2449-42T=	NP_000544.2:n.2449-42T=
XM_011544639.1:c.2368-42T=	XP_011542941.1:n.2368-42T=
XM_011544640.1:c.850-42T=	XP_011542942.1:n.850-42T=
XR_949470.1:n.2722-42T=
XR_949471.1:n.2722-42T=
XR_949472.1:n.2722-42T=
NM_000553.5:c.2449-42T=	NP_000544.2:n.2449-42T=
XM_011544639.3:c.2368-42T=	XP_011542941.1:n.2368-42T=
XM_024447265.1:c.2239-42T=	XP_024303033.1:n.2239-42T=
XR_949470.3:n.2750-42T=
XR_949471.3:n.2750-42T=
XR_949472.3:n.2750-42T=
NM_000553.6:c.2449-42T= MANE Select	NP_000544.2:n.2449-42T=