Canonical Allele Identifier: CA1647312201

Gene: EPHA7

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.93410921T= , CM000668.2:g.93410921T=	GRCh38
NC_000006.11:g.94120639T= , CM000668.1:g.94120639T=	GRCh37
NC_000006.10:g.94177360T=	NCBI36
NG_033944.1:g.13662A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004440.4:c.412A= MANE Select	NP_004431.1:p.Ile138=
ENST00000369303.9:c.412A= MANE Select	ENSP00000358309.4:p.Ile138=
NM_001288629.1:c.412A=	NP_001275558.1:p.Ile138=
NM_001288629.2:c.412A=	NP_001275558.1:p.Ile138=
NM_001288630.1:c.412A=	NP_001275559.1:p.Ile138=
NM_001288630.2:c.412A=	NP_001275559.1:p.Ile138=
NM_001376465.1:c.412A=	NP_001363394.1:p.Ile138=
NM_001376466.1:c.412A=	NP_001363395.1:p.Ile138=
NM_001376467.1:c.412A=	NP_001363396.1:p.Ile138=
NM_001376468.1:c.412A=	NP_001363397.1:p.Ile138=
NM_001376469.1:c.412A=	NP_001363398.1:p.Ile138=
NM_001376470.1:c.184A=	NP_001363399.1:p.Ile62=
NM_001376471.1:c.184A=	NP_001363400.1:p.Ile62=
NM_004440.3:c.412A=	NP_004431.1:p.Ile138=
NR_164810.1:n.630A=
ENST00000369297.1:c.412A=	ENSP00000358303.1:p.Ile138=
ENST00000369303.8:c.412A=	ENSP00000358309.4:p.Ile138=
ENST00000679565.1:c.412A=	ENSP00000506548.1:p.Ile138=
ENST00000679915.1:n.624A=
ENST00000680082.1:c.412A=	ENSP00000506654.1:p.Ile138=
ENST00000680190.1:c.184A=	ENSP00000505937.1:p.Ile62=
ENST00000680224.1:c.412A=	ENSP00000506130.1:p.Ile138=
ENST00000680473.1:n.650A=
ENST00000680550.1:n.623A=
ENST00000680953.1:c.184A=	ENSP00000505682.1:p.Ile62=
ENST00000681130.1:c.412A=	ENSP00000505801.1:p.Ile138=
ENST00000681287.1:n.630A=
ENST00000681503.1:n.625A=
ENST00000681532.1:c.412A=	ENSP00000505741.1:p.Ile138=
ENST00000681647.1:n.623A=
XM_005248669.1:c.412A=	XP_005248726.1:p.Ile138=
XM_005248669.3:c.412A=	XP_005248726.1:p.Ile138=
XM_005248671.1:c.412A=	XP_005248728.1:p.Ile138=
XM_005248671.3:c.412A=	XP_005248728.1:p.Ile138=
XM_017010365.2:c.412A=	XP_016865854.1:p.Ile138=
XM_017010366.2:c.412A=	XP_016865855.1:p.Ile138=
XR_001743218.2:n.655A=