Canonical Allele Identifier: CA2686839036

Gene: WRN

Linked Data

• dbSNP Id: rs2130416779
• gnomAD v4: 8-31141647-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141647C>T , CM000670.2:g.31141647C>T	GRCh38
NC_000008.10:g.30999163C>T , CM000670.1:g.30999163C>T	GRCh37
NC_000008.9:g.31118705C>T	NCBI36
NG_008870.1:g.113386C>T , LRG_524:g.113386C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3139-34C>T MANE Select	ENSP00000298139.5:n.3139-34C>T
ENST00000650667.1:c.*2753-34C>T	ENSP00000498593.1:n.*2753-34C>T
ENST00000298139.5:c.3139-34C>T	ENSP00000298139.5:n.3139-34C>T
ENST00000521620.5:n.1772-34C>T
NM_000553.4:c.3139-34C>T , LRG_524t1:c.3139-34C>T	NP_000544.2:n.3139-34C>T
XM_011544639.1:c.3058-34C>T	XP_011542941.1:n.3058-34C>T
XM_011544640.1:c.1540-34C>T	XP_011542942.1:n.1540-34C>T
XR_949470.1:n.3412-34C>T
XR_949471.1:n.3412-34C>T
XR_949472.1:n.3412-34C>T
NM_000553.5:c.3139-34C>T	NP_000544.2:n.3139-34C>T
XM_011544639.3:c.3058-34C>T	XP_011542941.1:n.3058-34C>T
XM_024447265.1:c.2929-34C>T	XP_024303033.1:n.2929-34C>T
XR_949470.3:n.3440-34C>T
XR_949471.3:n.3440-34C>T
XR_949472.3:n.3440-34C>T
NM_000553.6:c.3139-34C>T MANE Select	NP_000544.2:n.3139-34C>T