Canonical Allele Identifier: CA370918458

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31076215C>G , CM000670.2:g.31076215C>G	GRCh38
NC_000008.10:g.30933731C>G , CM000670.1:g.30933731C>G	GRCh37
NC_000008.9:g.31053273C>G	NCBI36
NG_008870.1:g.47954C>G , LRG_524:g.47954C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.767C>G MANE Select	NP_000544.2:p.Ser256Ter
ENST00000298139.7:c.767C>G MANE Select	ENSP00000298139.5:p.Ser256Ter
NM_000553.4:c.767C>G , LRG_524t1:c.767C>G	NP_000544.2:p.Ser256Ter
NM_000553.5:c.767C>G	NP_000544.2:p.Ser256Ter
ENST00000298139.5:c.767C>G	ENSP00000298139.5:p.Ser256Ter
ENST00000650667.1:c.*381C>G	ENSP00000498593.1:n.*381C>G
ENST00000651642.1:c.62C>G	ENSP00000498779.1:p.Ser21Ter
XM_011544639.1:c.767C>G	XP_011542941.1:p.Ser256Ter
XM_011544639.3:c.767C>G	XP_011542941.1:p.Ser256Ter
XM_024447265.1:c.557C>G	XP_024303033.1:p.Ser186Ter
XR_949470.1:n.1040C>G
XR_949470.3:n.1068C>G
XR_949471.1:n.1040C>G
XR_949471.3:n.1068C>G
XR_949472.1:n.1040C>G
XR_949472.3:n.1068C>G