Canonical Allele Identifier: CA735513669

Gene: EPHA10

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.37731169T>A , CM000663.2:g.37731169T>A	GRCh38
NC_000001.10:g.38196841T>A , CM000663.1:g.38196841T>A	GRCh37
NC_000001.9:g.37969428T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373048.9:c.1663+242A>T MANE Select	ENSP00000362139.4:n.1663+242A>T
ENST00000373048.8:c.1663+242A>T	ENSP00000362139.4:n.1663+242A>T
ENST00000427468.6:c.1663+242A>T	ENSP00000397746.2:n.1663+242A>T
ENST00000432874.7:c.84+242A>T
ENST00000437645.5:c.337+242A>T	ENSP00000432693.1:n.337+242A>T
ENST00000446149.6:n.462+242A>T
ENST00000525749.1:c.533+242A>T
ENST00000534097.5:c.163+242A>T	ENSP00000431389.1:n.163+242A>T
ENST00000540011.2:c.148+242A>T	ENSP00000441822.1:n.148+242A>T
NM_001099439.1:c.1663+242A>T	NP_001092909.1:n.1663+242A>T
XM_006710584.2:c.148+242A>T	XP_006710647.1:n.148+242A>T
XR_946610.1:n.400+242A>T
XR_946611.1:n.400+242A>T
XR_946612.1:n.400+242A>T
XR_946613.1:n.406+242A>T
XR_946614.1:n.400+242A>T
XM_017001080.1:c.472+242A>T	XP_016856569.1:n.472+242A>T
XM_017001081.1:c.472+242A>T	XP_016856570.1:n.472+242A>T
XR_001737123.1:n.491+242A>T
XR_001737124.1:n.491+242A>T
XR_001737125.2:n.346+242A>T
XR_001737126.1:n.491+242A>T
XR_001737127.1:n.491+242A>T
XR_946613.2:n.491+242A>T
NM_001099439.2:c.1663+242A>T MANE Select	NP_001092909.1:n.1663+242A>T