Canonical Allele Identifier: CA460221886

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30925782T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068266T>C , CM000670.2:g.31068266T>C	GRCh38
NC_000008.10:g.30925782T>C , CM000670.1:g.30925782T>C	GRCh37
NC_000008.9:g.31045324T>C	NCBI36
NG_008870.1:g.40005T>C , LRG_524:g.40005T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.663T>C MANE Select	ENSP00000298139.5:p.Phe221=
ENST00000650667.1:c.*277T>C	ENSP00000498593.1:n.*277T>C
ENST00000298139.5:c.663T>C	ENSP00000298139.5:p.Phe221=
NM_000553.4:c.663T>C , LRG_524t1:c.663T>C	NP_000544.2:p.Phe221=
XM_011544639.1:c.663T>C	XP_011542941.1:p.Phe221=
XR_949470.1:n.936T>C
XR_949471.1:n.936T>C
XR_949472.1:n.936T>C
NM_000553.5:c.663T>C	NP_000544.2:p.Phe221=
XM_011544639.3:c.663T>C	XP_011542941.1:p.Phe221=
XM_024447265.1:c.453T>C	XP_024303033.1:p.Phe151=
XR_949470.3:n.964T>C
XR_949471.3:n.964T>C
XR_949472.3:n.964T>C
NM_000553.6:c.663T>C MANE Select	NP_000544.2:p.Phe221=