Canonical Allele Identifier: CA1403750207

Gene: EPHB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.135090535C= , CM000665.2:g.135090535C=	GRCh38
NC_000003.11:g.134809377C= , CM000665.1:g.134809377C=	GRCh37
NC_000003.10:g.136292067C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398015.8:c.806-15913C= MANE Select	ENSP00000381097.3:n.806-15913C=
ENST00000647596.1:c.806-15913C=	ENSP00000497153.1:n.806-15913C=
ENST00000398015.7:c.806-15913C=	ENSP00000381097.3:n.806-15913C=
ENST00000482618.5:c.*72-15913C=	ENSP00000420338.1:n.*72-15913C=
ENST00000488154.5:n.472-15913C=
ENST00000493838.1:c.-512-15913C=	ENSP00000419574.1:n.-512-15913C=
NM_004441.4:c.806-15913C=	NP_004432.1:n.806-15913C=
XM_011512540.1:c.788-15913C=	XP_011510842.1:n.788-15913C=
XM_011512541.1:c.740-15913C=	XP_011510843.1:n.740-15913C=
XM_017005866.2:c.806-15913C=	XP_016861355.1:n.806-15913C=
XM_017005867.1:c.788-15913C=	XP_016861356.1:n.788-15913C=
XM_024453389.1:c.740-15913C=	XP_024309157.1:n.740-15913C=
XM_024453390.1:c.740-15913C=	XP_024309158.1:n.740-15913C=
NM_004441.5:c.806-15913C= MANE Select	NP_004432.1:n.806-15913C=