Canonical Allele Identifier: CA370912190

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31058505A>G , CM000670.2:g.31058505A>G	GRCh38
NC_000008.10:g.30916021A>G , CM000670.1:g.30916021A>G	GRCh37
NC_000008.9:g.31035563A>G	NCBI36
NG_008870.1:g.30244A>G , LRG_524:g.30244A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.58A>G MANE Select	NP_000544.2:p.Asn20Asp
ENST00000298139.7:c.58A>G MANE Select	ENSP00000298139.5:p.Asn20Asp
NM_000553.4:c.58A>G , LRG_524t1:c.58A>G	NP_000544.2:p.Asn20Asp
NM_000553.5:c.58A>G	NP_000544.2:p.Asn20Asp
ENST00000298139.5:c.58A>G	ENSP00000298139.5:p.Asn20Asp
ENST00000650667.1:c.58A>G	ENSP00000498593.1:p.Asn20Asp
XM_011544639.1:c.58A>G	XP_011542941.1:p.Asn20Asp
XM_011544639.3:c.58A>G	XP_011542941.1:p.Asn20Asp
XM_024447265.1:c.-277A>G	XP_024303033.1:n.-277A>G
XR_949470.1:n.331A>G
XR_949470.3:n.359A>G
XR_949471.1:n.331A>G
XR_949471.3:n.359A>G
XR_949472.1:n.331A>G
XR_949472.3:n.359A>G