Canonical Allele Identifier: CA1653702603

Gene: BEND3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.107079241C= , CM000668.2:g.107079241C=	GRCh38
NC_000006.11:g.107400445C= , CM000668.1:g.107400445C=	GRCh37
NC_000006.10:g.107507138C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369042.6:c.241-8291G= MANE Select	ENSP00000358038.1:n.241-8291G=
ENST00000369042.5:c.241-8291G=	ENSP00000358038.1:n.241-8291G=
ENST00000429433.3:c.241-8291G=	ENSP00000411268.2:n.241-8291G=
NM_001080450.2:c.241-8291G=	NP_001073919.1:n.241-8291G=
XM_005267079.2:c.241-8291G=	XP_005267136.1:n.241-8291G=
XM_005267080.2:c.241-8291G=	XP_005267137.1:n.241-8291G=
XM_011536005.1:c.241-8291G=	XP_011534307.1:n.241-8291G=
XM_011536006.1:c.241-8291G=	XP_011534308.1:n.241-8291G=
XM_011536007.1:c.241-8291G=	XP_011534309.1:n.241-8291G=
XM_005267079.4:c.241-8291G=	XP_005267136.1:n.241-8291G=
XM_005267080.4:c.241-8291G=	XP_005267137.1:n.241-8291G=
XM_011536005.3:c.241-8291G=	XP_011534307.1:n.241-8291G=
NM_001367314.1:c.241-8291G= MANE Select	NP_001354243.1:n.241-8291G=
NM_001080450.3:c.241-8291G=	NP_001073919.1:n.241-8291G=