Canonical Allele Identifier: CA460221601

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30924566C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067050C>T , CM000670.2:g.31067050C>T	GRCh38
NC_000008.10:g.30924566C>T , CM000670.1:g.30924566C>T	GRCh37
NC_000008.9:g.31044108C>T	NCBI36
NG_008870.1:g.38789C>T , LRG_524:g.38789C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.522C>T MANE Select	ENSP00000298139.5:p.Thr174=
ENST00000650667.1:c.*136C>T	ENSP00000498593.1:n.*136C>T
ENST00000298139.5:c.522C>T	ENSP00000298139.5:p.Thr174=
NM_000553.4:c.522C>T , LRG_524t1:c.522C>T	NP_000544.2:p.Thr174=
XM_011544639.1:c.522C>T	XP_011542941.1:p.Thr174=
XR_949470.1:n.795C>T
XR_949471.1:n.795C>T
XR_949472.1:n.795C>T
NM_000553.5:c.522C>T	NP_000544.2:p.Thr174=
XM_011544639.3:c.522C>T	XP_011542941.1:p.Thr174=
XM_024447265.1:c.312C>T	XP_024303033.1:p.Thr104=
XR_949470.3:n.823C>T
XR_949471.3:n.823C>T
XR_949472.3:n.823C>T
NM_000553.6:c.522C>T MANE Select	NP_000544.2:p.Thr174=