Canonical Allele Identifier: CA79988249
Gene: EPHA6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.96963418A>C , CM000665.2:g.96963418A>C GRCh38
NC_000003.11:g.96682262A>C , CM000665.1:g.96682262A>C GRCh37
NC_000003.10:g.98164952A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000389672.10:c.451-23912A>C MANE Select ENSP00000374323.5:n.451-23912A>C
ENST00000389672.9:c.451-23912A>C ENSP00000374323.5:n.451-23912A>C
ENST00000470610.6:c.451-23912A>C ENSP00000420598.2:n.451-23912A>C
ENST00000506569.1:c.284-23912A>C
NM_001080448.2:c.451-23912A>C NP_001073917.2:n.451-23912A>C
NM_001278301.1:c.451-23912A>C NP_001265230.1:n.451-23912A>C
XM_006713592.2:c.451-23912A>C XP_006713655.1:n.451-23912A>C
XM_011512705.1:c.451-23912A>C XP_011511007.1:n.451-23912A>C
XM_011512706.1:c.451-23912A>C XP_011511008.1:n.451-23912A>C
XM_011512707.1:c.451-23912A>C XP_011511009.1:n.451-23912A>C
XR_924126.1:n.494-23912A>C
NM_001080448.3:c.451-23912A>C MANE Select NP_001073917.2:n.451-23912A>C
XM_006713592.3:c.451-23912A>C XP_006713655.1:n.451-23912A>C
XM_011512705.2:c.451-23912A>C XP_011511007.1:n.451-23912A>C
XM_011512706.2:c.451-23912A>C XP_011511008.1:n.451-23912A>C
XM_011512707.2:c.451-23912A>C XP_011511009.1:n.451-23912A>C
XM_017006210.1:c.451-23912A>C XP_016861699.1:n.451-23912A>C
XM_017006211.1:c.66+14722A>C XP_016861700.1:n.66+14722A>C
XM_017006212.1:c.49-23912A>C XP_016861701.1:n.49-23912A>C
XM_017006214.1:c.25+96529A>C XP_016861703.1:n.25+96529A>C
XM_017006219.1:c.451-23912A>C XP_016861708.1:n.451-23912A>C
XR_001740110.1:n.494-23912A>C
XR_924126.2:n.494-23912A>C
NM_001278301.2:c.451-23912A>C NP_001265230.1:n.451-23912A>C
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