Canonical Allele Identifier: CA850744807

Gene: WRN

Linked Data

• dbSNP Id: rs1255957235
• gnomAD v4: 8-31154534-TA-T
• MyVariant Identifiers: chr8:g.31012051del (hg19) ; chr8:g.31154535del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31154535del , CM000670.2:g.31154535del	GRCh38
NC_000008.10:g.31012051del , CM000670.1:g.31012051del	GRCh37
NC_000008.9:g.31131593del	NCBI36
NG_008870.1:g.126274del , LRG_524:g.126274del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3688-89del MANE Select	ENSP00000298139.5:n.3688-89del
ENST00000650667.1:c.*3302-89del	ENSP00000498593.1:n.*3302-89del
ENST00000298139.5:c.3688-89del	ENSP00000298139.5:n.3688-89del
ENST00000521620.5:n.2321-89del
NM_000553.4:c.3688-89del , LRG_524t1:c.3688-89del	NP_000544.2:n.3688-89del
XM_011544639.1:c.3607-89del	XP_011542941.1:n.3607-89del
XM_011544640.1:c.2089-89del	XP_011542942.1:n.2089-89del
XR_949470.1:n.3961-89del
XR_949471.1:n.3961-89del
XR_949472.1:n.3961-89del
XR_949643.1:n.457-5870del
XR_949644.1:n.381-5870del
XR_949647.1:n.1070-5870del
XR_949648.1:n.972-5870del
NM_000553.5:c.3688-89del	NP_000544.2:n.3688-89del
XM_011544639.3:c.3607-89del	XP_011542941.1:n.3607-89del
XM_024447265.1:c.3478-89del	XP_024303033.1:n.3478-89del
XR_949470.3:n.3989-89del
XR_949471.3:n.3989-89del
XR_949472.3:n.3989-89del
NM_000553.6:c.3688-89del MANE Select	NP_000544.2:n.3688-89del