Canonical Allele Identifier: CA460221705

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30924653T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067137T>C , CM000670.2:g.31067137T>C	GRCh38
NC_000008.10:g.30924653T>C , CM000670.1:g.30924653T>C	GRCh37
NC_000008.9:g.31044195T>C	NCBI36
NG_008870.1:g.38876T>C , LRG_524:g.38876T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.609T>C MANE Select	ENSP00000298139.5:p.Phe203=
ENST00000650667.1:c.*223T>C	ENSP00000498593.1:n.*223T>C
ENST00000298139.5:c.609T>C	ENSP00000298139.5:p.Phe203=
NM_000553.4:c.609T>C , LRG_524t1:c.609T>C	NP_000544.2:p.Phe203=
XM_011544639.1:c.609T>C	XP_011542941.1:p.Phe203=
XR_949470.1:n.882T>C
XR_949471.1:n.882T>C
XR_949472.1:n.882T>C
NM_000553.5:c.609T>C	NP_000544.2:p.Phe203=
XM_011544639.3:c.609T>C	XP_011542941.1:p.Phe203=
XM_024447265.1:c.399T>C	XP_024303033.1:p.Phe133=
XR_949470.3:n.910T>C
XR_949471.3:n.910T>C
XR_949472.3:n.910T>C
NM_000553.6:c.609T>C MANE Select	NP_000544.2:p.Phe203=