Canonical Allele Identifier: CA368585830

Gene: EPHB4 SLC12A9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100827002G>T , CM000669.2:g.100827002G>T	GRCh38
NC_000007.13:g.100424624G>T , CM000669.1:g.100424624G>T	GRCh37
NC_000007.12:g.100262560G>T	NCBI36
NG_052671.1:g.5520C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358173.8:c.29C>A (EPHB4) MANE Select	ENSP00000350896.3:p.Ala10Asp
ENST00000358173.7:c.29C>A (EPHB4)	ENSP00000350896.3:p.Ala10Asp
ENST00000360620.7:c.29C>A (EPHB4)	ENSP00000353833.3:p.Ala10Asp
ENST00000461016.1:n.183G>T (SLC12A9)
ENST00000477446.5:n.29C>A (EPHB4)
ENST00000489808.1:n.29C>A (EPHB4)
ENST00000616502.4:c.29C>A (EPHB4)	ENSP00000482702.1:p.Ala10Asp
NM_004444.4:c.29C>A (EPHB4)	NP_004435.3:p.Ala10Asp
NM_001363494.1:c.-27G>T (SLC12A9)	NP_001350423.1:n.-27G>T
XM_017011816.1:c.29C>A (EPHB4)	XP_016867305.1:p.Ala10Asp
NM_004444.5:c.29C>A (EPHB4) MANE Select	NP_004435.3:p.Ala10Asp