Canonical Allele Identifier: CA11725329

Gene: EPHA5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.65605095T>C , CM000666.2:g.65605095T>C	GRCh38
NC_000004.11:g.66470813T>C , CM000666.1:g.66470813T>C	GRCh37
NC_000004.10:g.66153408T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613740.5:c.247-2791A>G MANE Select	ENSP00000478537.1:n.247-2791A>G
ENST00000273854.7:c.247-2791A>G	ENSP00000273854.3:n.247-2791A>G
ENST00000354839.8:c.247-2791A>G	ENSP00000346899.4:n.247-2791A>G
ENST00000432638.6:c.247-2791A>G	ENSP00000389208.2:n.247-2791A>G
ENST00000511294.1:c.247-2791A>G	ENSP00000427638.1:n.247-2791A>G
ENST00000613740.4:c.247-2791A>G	ENSP00000478537.1:n.247-2791A>G
ENST00000622150.4:c.247-2791A>G	ENSP00000480763.1:n.247-2791A>G
NM_001281765.1:c.247-2791A>G	NP_001268694.1:n.247-2791A>G
NM_001281766.1:c.247-2791A>G	NP_001268695.1:n.247-2791A>G
NM_001281767.1:c.247-2791A>G	NP_001268696.1:n.247-2791A>G
NM_004439.6:c.247-2791A>G	NP_004430.4:n.247-2791A>G
NM_182472.3:c.247-2791A>G	NP_872272.2:n.247-2791A>G
XM_005265653.2:c.247-2791A>G	XP_005265710.1:n.247-2791A>G
XM_011531733.1:c.40-2791A>G	XP_011530035.1:n.40-2791A>G
XM_011531734.1:c.40-2791A>G	XP_011530036.1:n.40-2791A>G
XM_011531735.1:c.247-2791A>G	XP_011530037.1:n.247-2791A>G
XM_011531736.1:c.247-2791A>G	XP_011530038.1:n.247-2791A>G
NM_001281765.2:c.247-2791A>G	NP_001268694.1:n.247-2791A>G
NM_001281766.2:c.247-2791A>G	NP_001268695.1:n.247-2791A>G
NM_001281767.2:c.247-2791A>G	NP_001268696.1:n.247-2791A>G
NM_001318761.1:c.40-2791A>G	NP_001305690.1:n.40-2791A>G
NM_004439.7:c.247-2791A>G	NP_004430.4:n.247-2791A>G
NM_182472.4:c.247-2791A>G	NP_872272.2:n.247-2791A>G
XM_005265653.4:c.247-2791A>G	XP_005265710.1:n.247-2791A>G
XM_011531735.3:c.247-2791A>G	XP_011530037.1:n.247-2791A>G
XM_017007878.2:c.247-2791A>G	XP_016863367.1:n.247-2791A>G
XM_017007879.2:c.247-2791A>G	XP_016863368.1:n.247-2791A>G
XM_017007880.2:c.247-2791A>G	XP_016863369.1:n.247-2791A>G
XM_017007881.2:c.247-2791A>G	XP_016863370.1:n.247-2791A>G
NM_001281767.3:c.247-2791A>G	NP_001268696.1:n.247-2791A>G
NM_004439.8:c.247-2791A>G	NP_004430.4:n.247-2791A>G
NM_182472.5:c.247-2791A>G	NP_872272.2:n.247-2791A>G
NM_001281765.3:c.247-2791A>G	NP_001268694.1:n.247-2791A>G
NM_001281766.3:c.247-2791A>G MANE Select	NP_001268695.1:n.247-2791A>G
NM_001318761.2:c.40-2791A>G	NP_001305690.1:n.40-2791A>G