Canonical Allele Identifier: CA174911273

Gene: WRN

Linked Data

• dbSNP Id: rs556165345
• gnomAD v3: 8-31154527-CTTGTG-C
• gnomAD v4: 8-31154527-CTTGTG-C
• MyVariant Identifiers: chr8:g.31012044_31012048del (hg19) ; chr8:g.31154528_31154532del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31154530_31154534del , CM000670.2:g.31154530_31154534del	GRCh38
NC_000008.10:g.31012046_31012050del , CM000670.1:g.31012046_31012050del	GRCh37
NC_000008.9:g.31131588_31131592del	NCBI36
NG_008870.1:g.126269_126273del , LRG_524:g.126269_126273del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.3688-94_3688-90del MANE Select	ENSP00000298139.5:n.3688-94_3688-90del
ENST00000650667.1:c.*3302-94_*3302-90del	ENSP00000498593.1:n.*3302-94_*3302-90del
ENST00000298139.5:c.3688-94_3688-90del	ENSP00000298139.5:n.3688-94_3688-90del
ENST00000521620.5:n.2321-94_2321-90del
NM_000553.4:c.3688-94_3688-90del , LRG_524t1:c.3688-94_3688-90del	NP_000544.2:n.3688-94_3688-90del
XM_011544639.1:c.3607-94_3607-90del	XP_011542941.1:n.3607-94_3607-90del
XM_011544640.1:c.2089-94_2089-90del	XP_011542942.1:n.2089-94_2089-90del
XR_949470.1:n.3961-94_3961-90del
XR_949471.1:n.3961-94_3961-90del
XR_949472.1:n.3961-94_3961-90del
XR_949643.1:n.457-5867_457-5863del
XR_949644.1:n.381-5867_381-5863del
XR_949647.1:n.1070-5867_1070-5863del
XR_949648.1:n.972-5867_972-5863del
NM_000553.5:c.3688-94_3688-90del	NP_000544.2:n.3688-94_3688-90del
XM_011544639.3:c.3607-94_3607-90del	XP_011542941.1:n.3607-94_3607-90del
XM_024447265.1:c.3478-94_3478-90del	XP_024303033.1:n.3478-94_3478-90del
XR_949470.3:n.3989-94_3989-90del
XR_949471.3:n.3989-94_3989-90del
XR_949472.3:n.3989-94_3989-90del
NM_000553.6:c.3688-94_3688-90del MANE Select	NP_000544.2:n.3688-94_3688-90del