Canonical Allele Identifier: CA370922997

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30999222A>G (hg19) ; chr8:g.31141706A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141706A>G , CM000670.2:g.31141706A>G	GRCh38
NC_000008.10:g.30999222A>G , CM000670.1:g.30999222A>G	GRCh37
NC_000008.9:g.31118764A>G	NCBI36
NG_008870.1:g.113445A>G , LRG_524:g.113445A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3164A>G MANE Select	ENSP00000298139.5:p.Asn1055Ser
ENST00000650667.1:c.*2778A>G	ENSP00000498593.1:n.*2778A>G
ENST00000298139.5:c.3164A>G	ENSP00000298139.5:p.Asn1055Ser
ENST00000521620.5:n.1797A>G
NM_000553.4:c.3164A>G , LRG_524t1:c.3164A>G	NP_000544.2:p.Asn1055Ser
XM_011544639.1:c.3083A>G	XP_011542941.1:p.Asn1028Ser
XM_011544640.1:c.1565A>G	XP_011542942.1:p.Asn522Ser
XR_949470.1:n.3437A>G
XR_949471.1:n.3437A>G
XR_949472.1:n.3437A>G
NM_000553.5:c.3164A>G	NP_000544.2:p.Asn1055Ser
XM_011544639.3:c.3083A>G	XP_011542941.1:p.Asn1028Ser
XM_024447265.1:c.2954A>G	XP_024303033.1:p.Asn985Ser
XR_949470.3:n.3465A>G
XR_949471.3:n.3465A>G
XR_949472.3:n.3465A>G
NM_000553.6:c.3164A>G MANE Select	NP_000544.2:p.Asn1055Ser