Canonical Allele Identifier: CA174889592

Gene: WRN

Linked Data

• dbSNP Id: rs373140422
• MyVariant Identifiers: chr8:g.31030653G>T (hg19) ; chr8:g.31173137G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173137G>T , CM000670.2:g.31173137G>T	GRCh38
NC_000008.10:g.31030653G>T , CM000670.1:g.31030653G>T	GRCh37
NC_000008.9:g.31150195G>T	NCBI36
NG_008870.1:g.144876G>T , LRG_524:g.144876G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.*35G>T MANE Select	ENSP00000298139.5:n.*35G>T
ENST00000650667.1:c.*3948G>T	ENSP00000498593.1:n.*3948G>T
ENST00000651946.1:n.558G>T
ENST00000298139.5:c.*35G>T	ENSP00000298139.5:n.*35G>T
ENST00000521620.5:n.2967G>T
NM_000553.4:c.*35G>T , LRG_524t1:c.*35G>T	NP_000544.2:n.*35G>T
XM_011544639.1:c.*35G>T	XP_011542941.1:n.*35G>T
XM_011544640.1:c.*35G>T	XP_011542942.1:n.*35G>T
XR_949643.1:n.88-1819C>A
XR_949644.1:n.88-1819C>A
XR_949645.1:n.88-1819C>A
XR_949646.1:n.88-1819C>A
XR_949647.1:n.701-1819C>A
XR_949648.1:n.603-1819C>A
NM_000553.5:c.*35G>T	NP_000544.2:n.*35G>T
XM_011544639.3:c.*35G>T	XP_011542941.1:n.*35G>T
XM_024447265.1:c.*35G>T	XP_024303033.1:n.*35G>T
NM_000553.6:c.*35G>T MANE Select	NP_000544.2:n.*35G>T