Canonical Allele Identifier: CA2234888729

Gene: WWOX

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099599A= , CM000678.2:g.78099599A=	GRCh38
NC_000016.9:g.78133496A= , CM000678.1:g.78133496A=	GRCh37
NC_000016.8:g.76690997A=	NCBI36
NG_011698.1:g.4946A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-180A=	ENSP00000485925.2:n.-180A=
ENST00000682609.1:n.148A=
ENST00000683286.1:n.148A=
ENST00000683929.1:c.-180A=	ENSP00000507689.1:n.-180A=
ENST00000684070.1:n.150A=
ENST00000684381.1:n.148A=
ENST00000684452.1:n.148A=
ENST00000684632.1:n.200A=
ENST00000566780.5:c.-180A=	ENSP00000457230.1:n.-180A=
ENST00000627394.2:c.-180A=	ENSP00000485925.1:n.-180A=
NM_001291997.1:c.-454A=	NP_001278926.1:n.-454A=
NM_016373.3:c.-180A=	NP_057457.1:n.-180A=
NM_130791.3:c.-180A=	NP_570607.1:n.-180A=
NR_120435.1:n.187A=
NR_120436.1:n.187A=