Canonical Allele Identifier: CA1403606558

Gene: EPHB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.134796494T= , CM000665.2:g.134796494T=	GRCh38
NC_000003.11:g.134515336T= , CM000665.1:g.134515336T=	GRCh37
NC_000003.10:g.135998026T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398015.8:c.58+805T= MANE Select	ENSP00000381097.3:n.58+805T=
ENST00000647596.1:c.58+805T=	ENSP00000497153.1:n.58+805T=
ENST00000398015.7:c.58+805T=	ENSP00000381097.3:n.58+805T=
ENST00000460895.5:c.-9+16613T=	ENSP00000417435.1:n.-9+16613T=
ENST00000482618.5:c.58+805T=	ENSP00000420338.1:n.58+805T=
ENST00000488154.5:n.58+805T=
ENST00000497173.5:c.-9+101T=	ENSP00000419688.1:n.-9+101T=
NM_004441.4:c.58+805T=	NP_004432.1:n.58+805T=
XM_017005866.2:c.58+805T=	XP_016861355.1:n.58+805T=
XM_024453389.1:c.-9+16613T=	XP_024309157.1:n.-9+16613T=
XM_024453390.1:c.-9+16613T=	XP_024309158.1:n.-9+16613T=
NM_004441.5:c.58+805T= MANE Select	NP_004432.1:n.58+805T=