Canonical Allele Identifier: CA370928803

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31154622A>G , CM000670.2:g.31154622A>G	GRCh38
NC_000008.10:g.31012138A>G , CM000670.1:g.31012138A>G	GRCh37
NC_000008.9:g.31131680A>G	NCBI36
NG_008870.1:g.126361A>G , LRG_524:g.126361A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.3688-2A>G MANE Select	NP_000544.2:n.3688-2A>G
ENST00000298139.7:c.3688-2A>G MANE Select	ENSP00000298139.5:n.3688-2A>G
NM_000553.4:c.3688-2A>G , LRG_524t1:c.3688-2A>G	NP_000544.2:n.3688-2A>G
NM_000553.5:c.3688-2A>G	NP_000544.2:n.3688-2A>G
ENST00000298139.5:c.3688-2A>G	ENSP00000298139.5:n.3688-2A>G
ENST00000521620.5:n.2321-2A>G
ENST00000650667.1:c.*3302-2A>G	ENSP00000498593.1:n.*3302-2A>G
XM_011544639.1:c.3607-2A>G	XP_011542941.1:n.3607-2A>G
XM_011544639.3:c.3607-2A>G	XP_011542941.1:n.3607-2A>G
XM_011544640.1:c.2089-2A>G	XP_011542942.1:n.2089-2A>G
XM_024447265.1:c.3478-2A>G	XP_024303033.1:n.3478-2A>G
XR_949470.1:n.3961-2A>G
XR_949470.3:n.3989-2A>G
XR_949471.1:n.3961-2A>G
XR_949471.3:n.3989-2A>G
XR_949472.1:n.3961-2A>G
XR_949472.3:n.3989-2A>G
XR_949643.1:n.457-5957T>C
XR_949644.1:n.381-5957T>C
XR_949647.1:n.1070-5957T>C
XR_949648.1:n.972-5957T>C