Canonical Allele Identifier: CA370922532

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30999098T>G (hg19) ; chr8:g.31141582T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141582T>G , CM000670.2:g.31141582T>G	GRCh38
NC_000008.10:g.30999098T>G , CM000670.1:g.30999098T>G	GRCh37
NC_000008.9:g.31118640T>G	NCBI36
NG_008870.1:g.113321T>G , LRG_524:g.113321T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.3120T>G MANE Select	ENSP00000298139.5:p.Ile1040Met
ENST00000650667.1:c.*2734T>G	ENSP00000498593.1:n.*2734T>G
ENST00000298139.5:c.3120T>G	ENSP00000298139.5:p.Ile1040Met
ENST00000521620.5:n.1753T>G
NM_000553.4:c.3120T>G , LRG_524t1:c.3120T>G	NP_000544.2:p.Ile1040Met
XM_011544639.1:c.3039T>G	XP_011542941.1:p.Ile1013Met
XM_011544640.1:c.1521T>G	XP_011542942.1:p.Ile507Met
XR_949470.1:n.3393T>G
XR_949471.1:n.3393T>G
XR_949472.1:n.3393T>G
NM_000553.5:c.3120T>G	NP_000544.2:p.Ile1040Met
XM_011544639.3:c.3039T>G	XP_011542941.1:p.Ile1013Met
XM_024447265.1:c.2910T>G	XP_024303033.1:p.Ile970Met
XR_949470.3:n.3421T>G
XR_949471.3:n.3421T>G
XR_949472.3:n.3421T>G
NM_000553.6:c.3120T>G MANE Select	NP_000544.2:p.Ile1040Met