Canonical Allele Identifier: CA460221760

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30924686C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067170C>G , CM000670.2:g.31067170C>G	GRCh38
NC_000008.10:g.30924686C>G , CM000670.1:g.30924686C>G	GRCh37
NC_000008.9:g.31044228C>G	NCBI36
NG_008870.1:g.38909C>G , LRG_524:g.38909C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.642C>G MANE Select	ENSP00000298139.5:p.Ala214=
ENST00000650667.1:c.*256C>G	ENSP00000498593.1:n.*256C>G
ENST00000298139.5:c.642C>G	ENSP00000298139.5:p.Ala214=
NM_000553.4:c.642C>G , LRG_524t1:c.642C>G	NP_000544.2:p.Ala214=
XM_011544639.1:c.642C>G	XP_011542941.1:p.Ala214=
XR_949470.1:n.915C>G
XR_949471.1:n.915C>G
XR_949472.1:n.915C>G
NM_000553.5:c.642C>G	NP_000544.2:p.Ala214=
XM_011544639.3:c.642C>G	XP_011542941.1:p.Ala214=
XM_024447265.1:c.432C>G	XP_024303033.1:p.Ala144=
XR_949470.3:n.943C>G
XR_949471.3:n.943C>G
XR_949472.3:n.943C>G
NM_000553.6:c.642C>G MANE Select	NP_000544.2:p.Ala214=