Canonical Allele Identifier: CA370915850

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31120418T>G , CM000670.2:g.31120418T>G	GRCh38
NC_000008.10:g.30977934T>G , CM000670.1:g.30977934T>G	GRCh37
NC_000008.9:g.31097476T>G	NCBI36
NG_008870.1:g.92157T>G , LRG_524:g.92157T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.2624T>G MANE Select	NP_000544.2:p.Leu875Ter
ENST00000298139.7:c.2624T>G MANE Select	ENSP00000298139.5:p.Leu875Ter
NM_000553.4:c.2624T>G , LRG_524t1:c.2624T>G	NP_000544.2:p.Leu875Ter
NM_000553.5:c.2624T>G	NP_000544.2:p.Leu875Ter
ENST00000298139.5:c.2624T>G	ENSP00000298139.5:p.Leu875Ter
ENST00000520169.1:n.463T>G
ENST00000521620.5:n.1257T>G
ENST00000650667.1:c.*2238T>G	ENSP00000498593.1:n.*2238T>G
XM_011544639.1:c.2543T>G	XP_011542941.1:p.Leu848Ter
XM_011544639.3:c.2543T>G	XP_011542941.1:p.Leu848Ter
XM_011544640.1:c.1025T>G	XP_011542942.1:p.Leu342Ter
XM_024447265.1:c.2414T>G	XP_024303033.1:p.Leu805Ter
XR_949470.1:n.2897T>G
XR_949470.3:n.2925T>G
XR_949471.1:n.2897T>G
XR_949471.3:n.2925T>G
XR_949472.1:n.2897T>G
XR_949472.3:n.2925T>G