Canonical Allele Identifier: CA460228396

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.31030546G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173030G>T , CM000670.2:g.31173030G>T	GRCh38
NC_000008.10:g.31030546G>T , CM000670.1:g.31030546G>T	GRCh37
NC_000008.9:g.31150088G>T	NCBI36
NG_008870.1:g.144769G>T , LRG_524:g.144769G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.4227G>T MANE Select	ENSP00000298139.5:p.Val1409=
ENST00000650667.1:c.*3841G>T	ENSP00000498593.1:n.*3841G>T
ENST00000651946.1:n.451G>T
ENST00000298139.5:c.4227G>T	ENSP00000298139.5:p.Val1409=
ENST00000521620.5:n.2860G>T
NM_000553.4:c.4227G>T , LRG_524t1:c.4227G>T	NP_000544.2:p.Val1409=
XM_011544639.1:c.4146G>T	XP_011542941.1:p.Val1382=
XM_011544640.1:c.2628G>T	XP_011542942.1:p.Val876=
XR_949643.1:n.88-1712C>A
XR_949644.1:n.88-1712C>A
XR_949645.1:n.88-1712C>A
XR_949646.1:n.88-1712C>A
XR_949647.1:n.701-1712C>A
XR_949648.1:n.603-1712C>A
NM_000553.5:c.4227G>T	NP_000544.2:p.Val1409=
XM_011544639.3:c.4146G>T	XP_011542941.1:p.Val1382=
XM_024447265.1:c.4017G>T	XP_024303033.1:p.Val1339=
NM_000553.6:c.4227G>T MANE Select	NP_000544.2:p.Val1409=