Canonical Allele Identifier: CA2581910559

Gene: EPHB1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.135197201G>A , CM000665.2:g.135197201G>A	GRCh38
NC_000003.11:g.134916043G>A , CM000665.1:g.134916043G>A	GRCh37
NC_000003.10:g.136398733G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398015.8:c.2131-4273G>A MANE Select	ENSP00000381097.3:n.2131-4273G>A
ENST00000647596.1:c.2131-4273G>A	ENSP00000497153.1:n.2131-4273G>A
ENST00000398015.7:c.2131-4273G>A	ENSP00000381097.3:n.2131-4273G>A
ENST00000493838.1:c.814-4273G>A	ENSP00000419574.1:n.814-4273G>A
NM_004441.4:c.2131-4273G>A	NP_004432.1:n.2131-4273G>A
XM_011512540.1:c.2113-4273G>A	XP_011510842.1:n.2113-4273G>A
XM_011512541.1:c.2065-4273G>A	XP_011510843.1:n.2065-4273G>A
XM_011512542.1:c.361-4273G>A	XP_011510844.1:n.361-4273G>A
XM_017005866.2:c.2293-4273G>A	XP_016861355.1:n.2293-4273G>A
XM_017005867.1:c.2275-4273G>A	XP_016861356.1:n.2275-4273G>A
XM_024453389.1:c.2227-4273G>A	XP_024309157.1:n.2227-4273G>A
XM_024453390.1:c.2227-4273G>A	XP_024309158.1:n.2227-4273G>A
NM_004441.5:c.2131-4273G>A MANE Select	NP_004432.1:n.2131-4273G>A