Canonical Allele Identifier: CA370925165

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.31004575G>T (hg19) ; chr8:g.31147059G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147059G>T , CM000670.2:g.31147059G>T	GRCh38
NC_000008.10:g.31004575G>T , CM000670.1:g.31004575G>T	GRCh37
NC_000008.9:g.31124117G>T	NCBI36
NG_008870.1:g.118798G>T , LRG_524:g.118798G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3390G>T MANE Select	ENSP00000298139.5:p.Met1130Ile
ENST00000650667.1:c.*3004G>T	ENSP00000498593.1:n.*3004G>T
ENST00000298139.5:c.3390G>T	ENSP00000298139.5:p.Met1130Ile
ENST00000521620.5:n.2023G>T
NM_000553.4:c.3390G>T , LRG_524t1:c.3390G>T	NP_000544.2:p.Met1130Ile
XM_011544639.1:c.3309G>T	XP_011542941.1:p.Met1103Ile
XM_011544640.1:c.1791G>T	XP_011542942.1:p.Met597Ile
XR_949470.1:n.3663G>T
XR_949471.1:n.3663G>T
XR_949472.1:n.3663G>T
XR_949643.1:n.614+1449C>A
NM_000553.5:c.3390G>T	NP_000544.2:p.Met1130Ile
XM_011544639.3:c.3309G>T	XP_011542941.1:p.Met1103Ile
XM_024447265.1:c.3180G>T	XP_024303033.1:p.Met1060Ile
XR_949470.3:n.3691G>T
XR_949471.3:n.3691G>T
XR_949472.3:n.3691G>T
NM_000553.6:c.3390G>T MANE Select	NP_000544.2:p.Met1130Ile