Canonical Allele Identifier: CA2830544767

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141664_31141671del , CM000670.2:g.31141664_31141671del	GRCh38
NC_000008.10:g.30999180_30999187del , CM000670.1:g.30999180_30999187del	GRCh37
NC_000008.9:g.31118722_31118729del	NCBI36
NG_008870.1:g.113403_113410del , LRG_524:g.113403_113410del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3139-17_3139-10del MANE Select	ENSP00000298139.5:n.3139-17_3139-10del
ENST00000650667.1:c.*2753-17_*2753-10del	ENSP00000498593.1:n.*2753-17_*2753-10del
ENST00000298139.5:c.3139-17_3139-10del	ENSP00000298139.5:n.3139-17_3139-10del
ENST00000521620.5:n.1772-17_1772-10del
NM_000553.4:c.3139-17_3139-10del , LRG_524t1:c.3139-17_3139-10del	NP_000544.2:n.3139-17_3139-10del
XM_011544639.1:c.3058-17_3058-10del	XP_011542941.1:n.3058-17_3058-10del
XM_011544640.1:c.1540-17_1540-10del	XP_011542942.1:n.1540-17_1540-10del
XR_949470.1:n.3412-17_3412-10del
XR_949471.1:n.3412-17_3412-10del
XR_949472.1:n.3412-17_3412-10del
NM_000553.5:c.3139-17_3139-10del	NP_000544.2:n.3139-17_3139-10del
XM_011544639.3:c.3058-17_3058-10del	XP_011542941.1:n.3058-17_3058-10del
XM_024447265.1:c.2929-17_2929-10del	XP_024303033.1:n.2929-17_2929-10del
XR_949470.3:n.3440-17_3440-10del
XR_949471.3:n.3440-17_3440-10del
XR_949472.3:n.3440-17_3440-10del
NM_000553.6:c.3139-17_3139-10del MANE Select	NP_000544.2:n.3139-17_3139-10del