Canonical Allele Identifier: CA370923206

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30999287C>A (hg19) ; chr8:g.31141771C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141771C>A , CM000670.2:g.31141771C>A	GRCh38
NC_000008.10:g.30999287C>A , CM000670.1:g.30999287C>A	GRCh37
NC_000008.9:g.31118829C>A	NCBI36
NG_008870.1:g.113510C>A , LRG_524:g.113510C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.3229C>A MANE Select	ENSP00000298139.5:p.Pro1077Thr
ENST00000650667.1:c.*2843C>A	ENSP00000498593.1:n.*2843C>A
ENST00000298139.5:c.3229C>A	ENSP00000298139.5:p.Pro1077Thr
ENST00000521620.5:n.1862C>A
NM_000553.4:c.3229C>A , LRG_524t1:c.3229C>A	NP_000544.2:p.Pro1077Thr
XM_011544639.1:c.3148C>A	XP_011542941.1:p.Pro1050Thr
XM_011544640.1:c.1630C>A	XP_011542942.1:p.Pro544Thr
XR_949470.1:n.3502C>A
XR_949471.1:n.3502C>A
XR_949472.1:n.3502C>A
NM_000553.5:c.3229C>A	NP_000544.2:p.Pro1077Thr
XM_011544639.3:c.3148C>A	XP_011542941.1:p.Pro1050Thr
XM_024447265.1:c.3019C>A	XP_024303033.1:p.Pro1007Thr
XR_949470.3:n.3530C>A
XR_949471.3:n.3530C>A
XR_949472.3:n.3530C>A
NM_000553.6:c.3229C>A MANE Select	NP_000544.2:p.Pro1077Thr