Canonical Allele Identifier: CA2686840055

Gene: WRN

Linked Data

• gnomAD v4: 8-31154531-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31154531T>C , CM000670.2:g.31154531T>C	GRCh38
NC_000008.10:g.31012047T>C , CM000670.1:g.31012047T>C	GRCh37
NC_000008.9:g.31131589T>C	NCBI36
NG_008870.1:g.126270T>C , LRG_524:g.126270T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.3688-93T>C MANE Select	ENSP00000298139.5:n.3688-93T>C
ENST00000650667.1:c.*3302-93T>C	ENSP00000498593.1:n.*3302-93T>C
ENST00000298139.5:c.3688-93T>C	ENSP00000298139.5:n.3688-93T>C
ENST00000521620.5:n.2321-93T>C
NM_000553.4:c.3688-93T>C , LRG_524t1:c.3688-93T>C	NP_000544.2:n.3688-93T>C
XM_011544639.1:c.3607-93T>C	XP_011542941.1:n.3607-93T>C
XM_011544640.1:c.2089-93T>C	XP_011542942.1:n.2089-93T>C
XR_949470.1:n.3961-93T>C
XR_949471.1:n.3961-93T>C
XR_949472.1:n.3961-93T>C
XR_949643.1:n.457-5866A>G
XR_949644.1:n.381-5866A>G
XR_949647.1:n.1070-5866A>G
XR_949648.1:n.972-5866A>G
NM_000553.5:c.3688-93T>C	NP_000544.2:n.3688-93T>C
XM_011544639.3:c.3607-93T>C	XP_011542941.1:n.3607-93T>C
XM_024447265.1:c.3478-93T>C	XP_024303033.1:n.3478-93T>C
XR_949470.3:n.3989-93T>C
XR_949471.3:n.3989-93T>C
XR_949472.3:n.3989-93T>C
NM_000553.6:c.3688-93T>C MANE Select	NP_000544.2:n.3688-93T>C