Canonical Allele Identifier: CA15545029

Gene: WRN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31078840G>T , CM000670.2:g.31078840G>T	GRCh38
NC_000008.10:g.30936356G>T , CM000670.1:g.30936356G>T	GRCh37
NC_000008.9:g.31055898G>T	NCBI36
NG_008870.1:g.50579G>T , LRG_524:g.50579G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.840-2027G>T MANE Select	ENSP00000298139.5:n.840-2027G>T
ENST00000650667.1:c.*454-2027G>T	ENSP00000498593.1:n.*454-2027G>T
ENST00000651642.1:c.135-2027G>T	ENSP00000498779.1:n.135-2027G>T
ENST00000298139.5:c.840-2027G>T	ENSP00000298139.5:n.840-2027G>T
NM_000553.4:c.840-2027G>T , LRG_524t1:c.840-2027G>T	NP_000544.2:n.840-2027G>T
XM_011544639.1:c.840-2027G>T	XP_011542941.1:n.840-2027G>T
XR_949470.1:n.1113-2027G>T
XR_949471.1:n.1113-2027G>T
XR_949472.1:n.1113-2027G>T
NM_000553.5:c.840-2027G>T	NP_000544.2:n.840-2027G>T
XM_011544639.3:c.840-2027G>T	XP_011542941.1:n.840-2027G>T
XM_024447265.1:c.630-2027G>T	XP_024303033.1:n.630-2027G>T
XR_949470.3:n.1141-2027G>T
XR_949471.3:n.1141-2027G>T
XR_949472.3:n.1141-2027G>T
NM_000553.6:c.840-2027G>T MANE Select	NP_000544.2:n.840-2027G>T