Canonical Allele Identifier: CA1403654946

Gene: EPHB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.134951682C= , CM000665.2:g.134951682C=	GRCh38
NC_000003.11:g.134670524C= , CM000665.1:g.134670524C=	GRCh37
NC_000003.10:g.136153214C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398015.8:c.435C= MANE Select	ENSP00000381097.3:p.Ser145=
ENST00000647596.1:c.435C=	ENSP00000497153.1:p.Ser145=
ENST00000398015.7:c.435C=	ENSP00000381097.3:p.Ser145=
ENST00000474732.1:c.369C=	ENSP00000418352.1:p.Ser123=
ENST00000482618.5:c.435C=	ENSP00000420338.1:p.Ser145=
ENST00000488154.5:n.435C=
NM_004441.4:c.435C=	NP_004432.1:p.Ser145=
XM_011512540.1:c.417C=	XP_011510842.1:p.Ser139=
XM_011512541.1:c.369C=	XP_011510843.1:p.Ser123=
XM_017005866.2:c.435C=	XP_016861355.1:p.Ser145=
XM_017005867.1:c.417C=	XP_016861356.1:p.Ser139=
XM_024453389.1:c.369C=	XP_024309157.1:p.Ser123=
XM_024453390.1:c.369C=	XP_024309158.1:p.Ser123=
NM_004441.5:c.435C= MANE Select	NP_004432.1:p.Ser145=