Canonical Allele Identifier: CA80026213

Gene: EPHA6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.97291143T>C , CM000665.2:g.97291143T>C	GRCh38
NC_000003.11:g.97009987T>C , CM000665.1:g.97009987T>C	GRCh37
NC_000003.10:g.98492677T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389672.10:c.1606+46856T>C MANE Select	ENSP00000374323.5:n.1606+46856T>C
ENST00000389672.9:c.1606+46856T>C	ENSP00000374323.5:n.1606+46856T>C
NM_001080448.2:c.1606+46856T>C	NP_001073917.2:n.1606+46856T>C
XM_006713592.2:c.1606+46856T>C	XP_006713655.1:n.1606+46856T>C
XR_924126.1:n.1650-19116T>C
XR_924241.1:n.682-3099A>G
NM_001080448.3:c.1606+46856T>C MANE Select	NP_001073917.2:n.1606+46856T>C
XM_006713592.3:c.1606+46856T>C	XP_006713655.1:n.1606+46856T>C
XM_017006210.1:c.1606+46856T>C	XP_016861699.1:n.1606+46856T>C
XM_017006211.1:c.1222+46856T>C	XP_016861700.1:n.1222+46856T>C
XM_017006212.1:c.1204+46856T>C	XP_016861701.1:n.1204+46856T>C
XM_017006213.1:c.1138+46856T>C	XP_016861702.1:n.1138+46856T>C
XM_017006214.1:c.517+46856T>C	XP_016861703.1:n.517+46856T>C
XM_017006218.1:c.3+46856T>C	XP_016861707.1:n.3+46856T>C
XM_017006219.1:c.1606+46856T>C	XP_016861708.1:n.1606+46856T>C
XR_001740110.1:n.1649+46856T>C
XR_924126.2:n.1650-19116T>C