Canonical Allele Identifier: CA1647271969

Gene: EPHA7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.93298794C= , CM000668.2:g.93298794C=	GRCh38
NC_000006.11:g.94008512C= , CM000668.1:g.94008512C=	GRCh37
NC_000006.10:g.94065233C=	NCBI36
NG_033944.1:g.125789G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369303.9:c.1325-26372G= MANE Select	ENSP00000358309.4:n.1325-26372G=
ENST00000679565.1:c.1325-26372G=	ENSP00000506548.1:n.1325-26372G=
ENST00000679915.1:n.1537-26372G=
ENST00000680082.1:c.1325-26372G=	ENSP00000506654.1:n.1325-26372G=
ENST00000680190.1:c.1097-26372G=	ENSP00000505937.1:n.1097-26372G=
ENST00000680224.1:c.1325-26372G=	ENSP00000506130.1:n.1325-26372G=
ENST00000680473.1:n.1563-26372G=
ENST00000680813.1:n.567-26372G=
ENST00000680953.1:c.1097-26372G=	ENSP00000505682.1:n.1097-26372G=
ENST00000681130.1:c.1325-26372G=	ENSP00000505801.1:n.1325-26372G=
ENST00000681532.1:c.1325-26372G=	ENSP00000505741.1:n.1325-26372G=
ENST00000681647.1:n.1536-14410G=
ENST00000369303.8:c.1325-26372G=	ENSP00000358309.4:n.1325-26372G=
NM_001288629.1:c.1325-26372G=	NP_001275558.1:n.1325-26372G=
NM_004440.3:c.1325-26372G=	NP_004431.1:n.1325-26372G=
XM_005248669.1:c.1325-26372G=	XP_005248726.1:n.1325-26372G=
XM_005248671.1:c.1325-26372G=	XP_005248728.1:n.1325-26372G=
XM_005248669.3:c.1325-26372G=	XP_005248726.1:n.1325-26372G=
XM_005248671.3:c.1325-26372G=	XP_005248728.1:n.1325-26372G=
XM_017010365.2:c.1325-26372G=	XP_016865854.1:n.1325-26372G=
XR_001743218.2:n.1568-26372G=
NM_004440.4:c.1325-26372G= MANE Select	NP_004431.1:n.1325-26372G=
NM_001288629.2:c.1325-26372G=	NP_001275558.1:n.1325-26372G=
NM_001376465.1:c.1325-26372G=	NP_001363394.1:n.1325-26372G=
NM_001376466.1:c.1325-26372G=	NP_001363395.1:n.1325-26372G=
NM_001376467.1:c.1325-26372G=	NP_001363396.1:n.1325-26372G=
NM_001376468.1:c.1325-26372G=	NP_001363397.1:n.1325-26372G=
NM_001376470.1:c.1097-26372G=	NP_001363399.1:n.1097-26372G=
NM_001376471.1:c.1097-26372G=	NP_001363400.1:n.1097-26372G=
NR_164810.1:n.1543-26372G=