Canonical Allele Identifier: CA80043851

Gene: EPHA6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.97449896A>T , CM000665.2:g.97449896A>T	GRCh38
NC_000003.11:g.97168740A>T , CM000665.1:g.97168740A>T	GRCh37
NC_000003.10:g.98651430A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389672.10:c.1894+1166A>T MANE Select	ENSP00000374323.5:n.1894+1166A>T
ENST00000389672.9:c.1894+1166A>T	ENSP00000374323.5:n.1894+1166A>T
ENST00000477384.6:c.-9+1166A>T	ENSP00000419470.2:n.-9+1166A>T
ENST00000502694.1:c.6+1166A>T	ENSP00000423950.1:n.6+1166A>T
ENST00000503760.5:c.6+1166A>T	ENSP00000421260.1:n.6+1166A>T
ENST00000508345.5:c.-9+1166A>T	ENSP00000424638.1:n.-9+1166A>T
ENST00000514100.5:c.6+1166A>T	ENSP00000421711.1:n.6+1166A>T
NM_001080448.2:c.1894+1166A>T	NP_001073917.2:n.1894+1166A>T
NM_001278300.1:c.6+1166A>T	NP_001265229.1:n.6+1166A>T
NM_173655.3:c.6+1166A>T	NP_775926.1:n.6+1166A>T
XM_006713592.2:c.1942+1166A>T	XP_006713655.1:n.1942+1166A>T
XR_924127.1:n.285+1166A>T
NM_001080448.3:c.1894+1166A>T MANE Select	NP_001073917.2:n.1894+1166A>T
XM_006713592.3:c.1942+1166A>T	XP_006713655.1:n.1942+1166A>T
XM_017006210.1:c.1942+1166A>T	XP_016861699.1:n.1942+1166A>T
XM_017006211.1:c.1558+1166A>T	XP_016861700.1:n.1558+1166A>T
XM_017006212.1:c.1540+1166A>T	XP_016861701.1:n.1540+1166A>T
XM_017006213.1:c.1474+1166A>T	XP_016861702.1:n.1474+1166A>T
XM_017006214.1:c.853+1166A>T	XP_016861703.1:n.853+1166A>T
XM_017006215.1:c.286+1166A>T	XP_016861704.1:n.286+1166A>T
XM_017006216.1:c.238+1166A>T	XP_016861705.1:n.238+1166A>T
XM_017006217.1:c.166+1166A>T	XP_016861706.1:n.166+1166A>T
XM_017006218.1:c.166+1166A>T	XP_016861707.1:n.166+1166A>T
XM_017006220.1:c.6+1166A>T	XP_016861709.1:n.6+1166A>T
XM_017006223.1:c.6+1166A>T	XP_016861712.1:n.6+1166A>T
XR_001740110.1:n.1985+1166A>T
NM_001278300.2:c.6+1166A>T	NP_001265229.1:n.6+1166A>T
NM_173655.4:c.6+1166A>T	NP_775926.1:n.6+1166A>T