Canonical Allele Identifier: CA2686840054

Gene: WRN

Linked Data

• gnomAD v4: 8-31154527-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31154527C>A , CM000670.2:g.31154527C>A	GRCh38
NC_000008.10:g.31012043C>A , CM000670.1:g.31012043C>A	GRCh37
NC_000008.9:g.31131585C>A	NCBI36
NG_008870.1:g.126266C>A , LRG_524:g.126266C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3688-97C>A MANE Select	ENSP00000298139.5:n.3688-97C>A
ENST00000650667.1:c.*3302-97C>A	ENSP00000498593.1:n.*3302-97C>A
ENST00000298139.5:c.3688-97C>A	ENSP00000298139.5:n.3688-97C>A
ENST00000521620.5:n.2321-97C>A
NM_000553.4:c.3688-97C>A , LRG_524t1:c.3688-97C>A	NP_000544.2:n.3688-97C>A
XM_011544639.1:c.3607-97C>A	XP_011542941.1:n.3607-97C>A
XM_011544640.1:c.2089-97C>A	XP_011542942.1:n.2089-97C>A
XR_949470.1:n.3961-97C>A
XR_949471.1:n.3961-97C>A
XR_949472.1:n.3961-97C>A
XR_949643.1:n.457-5862G>T
XR_949644.1:n.381-5862G>T
XR_949647.1:n.1070-5862G>T
XR_949648.1:n.972-5862G>T
NM_000553.5:c.3688-97C>A	NP_000544.2:n.3688-97C>A
XM_011544639.3:c.3607-97C>A	XP_011542941.1:n.3607-97C>A
XM_024447265.1:c.3478-97C>A	XP_024303033.1:n.3478-97C>A
XR_949470.3:n.3989-97C>A
XR_949471.3:n.3989-97C>A
XR_949472.3:n.3989-97C>A
NM_000553.6:c.3688-97C>A MANE Select	NP_000544.2:n.3688-97C>A