Canonical Allele Identifier: CA1382614874

Gene: EPHA3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.89356604A= , CM000665.2:g.89356604A=	GRCh38
NC_000003.11:g.89405754A= , CM000665.1:g.89405754A=	GRCh37
NC_000003.10:g.89488444A=	NCBI36
NG_023239.1:g.254081A=
NG_023239.2:g.254081A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336596.7:c.1306+14514A= MANE Select	ENSP00000337451.2:n.1306+14514A=
ENST00000336596.6:c.1306+14514A=	ENSP00000337451.2:n.1306+14514A=
ENST00000452448.6:c.1306+14514A=	ENSP00000399926.2:n.1306+14514A=
ENST00000494014.1:c.1306+14514A=	ENSP00000419190.1:n.1306+14514A=
NM_005233.5:c.1306+14514A=	NP_005224.2:n.1306+14514A=
NM_182644.2:c.1306+14514A=	NP_872585.1:n.1306+14514A=
XM_005264715.1:c.1306+14514A=	XP_005264772.1:n.1306+14514A=
XM_005264716.1:c.1306+14514A=	XP_005264773.1:n.1306+14514A=
XM_005264715.3:c.1306+14514A=	XP_005264772.1:n.1306+14514A=
XM_005264716.3:c.1306+14514A=	XP_005264773.1:n.1306+14514A=
NM_005233.6:c.1306+14514A= MANE Select	NP_005224.2:n.1306+14514A=
NM_182644.3:c.1306+14514A=	NP_872585.1:n.1306+14514A=