Canonical Allele Identifier: CA460488463

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30999202A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141686A>G , CM000670.2:g.31141686A>G	GRCh38
NC_000008.10:g.30999202A>G , CM000670.1:g.30999202A>G	GRCh37
NC_000008.9:g.31118744A>G	NCBI36
NG_008870.1:g.113425A>G , LRG_524:g.113425A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.3144A>G MANE Select	ENSP00000298139.5:p.Arg1048=
ENST00000650667.1:c.*2758A>G	ENSP00000498593.1:n.*2758A>G
ENST00000298139.5:c.3144A>G	ENSP00000298139.5:p.Arg1048=
ENST00000521620.5:n.1777A>G
NM_000553.4:c.3144A>G , LRG_524t1:c.3144A>G	NP_000544.2:p.Arg1048=
XM_011544639.1:c.3063A>G	XP_011542941.1:p.Arg1021=
XM_011544640.1:c.1545A>G	XP_011542942.1:p.Arg515=
XR_949470.1:n.3417A>G
XR_949471.1:n.3417A>G
XR_949472.1:n.3417A>G
NM_000553.5:c.3144A>G	NP_000544.2:p.Arg1048=
XM_011544639.3:c.3063A>G	XP_011542941.1:p.Arg1021=
XM_024447265.1:c.2934A>G	XP_024303033.1:p.Arg978=
XR_949470.3:n.3445A>G
XR_949471.3:n.3445A>G
XR_949472.3:n.3445A>G
NM_000553.6:c.3144A>G MANE Select	NP_000544.2:p.Arg1048=