Canonical Allele Identifier: CA162779

Gene: WRN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173019C>T , CM000670.2:g.31173019C>T	GRCh38
NC_000008.10:g.31030535C>T , CM000670.1:g.31030535C>T	GRCh37
NC_000008.9:g.31150077C>T	NCBI36
NG_008870.1:g.144758C>T , LRG_524:g.144758C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.4216C>T MANE Select	ENSP00000298139.5:p.Arg1406Ter
ENST00000650667.1:c.*3830C>T	ENSP00000498593.1:n.*3830C>T
ENST00000651946.1:n.440C>T
ENST00000298139.5:c.4216C>T	ENSP00000298139.5:p.Arg1406Ter
ENST00000521620.5:n.2849C>T
NM_000553.4:c.4216C>T , LRG_524t1:c.4216C>T	NP_000544.2:p.Arg1406Ter
XM_011544639.1:c.4135C>T	XP_011542941.1:p.Arg1379Ter
XM_011544640.1:c.2617C>T	XP_011542942.1:p.Arg873Ter
XR_949643.1:n.88-1701G>A
XR_949644.1:n.88-1701G>A
XR_949645.1:n.88-1701G>A
XR_949646.1:n.88-1701G>A
XR_949647.1:n.701-1701G>A
XR_949648.1:n.603-1701G>A
NM_000553.5:c.4216C>T	NP_000544.2:p.Arg1406Ter
XM_011544639.3:c.4135C>T	XP_011542941.1:p.Arg1379Ter
XM_024447265.1:c.4006C>T	XP_024303033.1:p.Arg1336Ter
NM_000553.6:c.4216C>T MANE Select	NP_000544.2:p.Arg1406Ter