Canonical Allele Identifier: CA1386733367

Gene: EPHA6

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.97192120C>G , CM000665.2:g.97192120C>G	GRCh38
NC_000003.11:g.96910964C>G , CM000665.1:g.96910964C>G	GRCh37
NC_000003.10:g.98393654C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389672.10:c.1115-34144C>G MANE Select	ENSP00000374323.5:n.1115-34144C>G
ENST00000389672.9:c.1115-34144C>G	ENSP00000374323.5:n.1115-34144C>G
ENST00000470610.6:c.1115-34144C>G	ENSP00000420598.2:n.1115-34144C>G
NM_001080448.2:c.1115-34144C>G	NP_001073917.2:n.1115-34144C>G
XM_006713592.2:c.1115-34144C>G	XP_006713655.1:n.1115-34144C>G
XR_924126.1:n.1158-34144C>G
NM_001080448.3:c.1115-34144C>G MANE Select	NP_001073917.2:n.1115-34144C>G
XM_006713592.3:c.1115-34144C>G	XP_006713655.1:n.1115-34144C>G
XM_017006210.1:c.1115-34144C>G	XP_016861699.1:n.1115-34144C>G
XM_017006211.1:c.731-34144C>G	XP_016861700.1:n.731-34144C>G
XM_017006212.1:c.713-34144C>G	XP_016861701.1:n.713-34144C>G
XM_017006213.1:c.647-34144C>G	XP_016861702.1:n.647-34144C>G
XM_017006214.1:c.26-34144C>G	XP_016861703.1:n.26-34144C>G
XM_017006219.1:c.1115-34144C>G	XP_016861708.1:n.1115-34144C>G
XR_001740110.1:n.1158-34144C>G
XR_924126.2:n.1158-34144C>G