Canonical Allele Identifier: CA357052956

Gene: EPHA5

Linked Data

• dbSNP Id: rs1057520012
• MyVariant Identifiers: chr4:g.66270137C>G (hg19) ; chr4:g.65404419C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.65404419C>G , CM000666.2:g.65404419C>G	GRCh38
NC_000004.11:g.66270137C>G , CM000666.1:g.66270137C>G	GRCh37
NC_000004.10:g.65952732C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000613740.5:c.1748G>C MANE Select	ENSP00000478537.1:p.Gly583Ala
ENST00000273854.7:c.1745G>C	ENSP00000273854.3:p.Gly582Ala
ENST00000354839.8:c.1745G>C	ENSP00000346899.4:p.Gly582Ala
ENST00000432638.6:c.1256G>C	ENSP00000389208.2:p.Gly419Ala
ENST00000511294.1:c.1748G>C	ENSP00000427638.1:p.Gly583Ala
ENST00000613740.4:c.1748G>C	ENSP00000478537.1:p.Gly583Ala
ENST00000622150.4:c.1748G>C	ENSP00000480763.1:p.Gly583Ala
NM_001281765.1:c.1748G>C	NP_001268694.1:p.Gly583Ala
NM_001281766.1:c.1748G>C	NP_001268695.1:p.Gly583Ala
NM_001281767.1:c.1748G>C	NP_001268696.1:p.Gly583Ala
NM_004439.6:c.1745G>C	NP_004430.4:p.Gly582Ala
NM_182472.3:c.1745G>C	NP_872272.2:p.Gly582Ala
XM_005265653.2:c.1256G>C	XP_005265710.1:p.Gly419Ala
XM_011531733.1:c.1541G>C	XP_011530035.1:p.Gly514Ala
XM_011531734.1:c.1541G>C	XP_011530036.1:p.Gly514Ala
XM_011531735.1:c.1412G>C	XP_011530037.1:p.Gly471Ala
XM_011531736.1:c.1748G>C	XP_011530038.1:p.Gly583Ala
NM_001281765.2:c.1748G>C	NP_001268694.1:p.Gly583Ala
NM_001281766.2:c.1748G>C	NP_001268695.1:p.Gly583Ala
NM_001281767.2:c.1748G>C	NP_001268696.1:p.Gly583Ala
NM_001318761.1:c.1541G>C	NP_001305690.1:p.Gly514Ala
NM_004439.7:c.1745G>C	NP_004430.4:p.Gly582Ala
NM_182472.4:c.1745G>C	NP_872272.2:p.Gly582Ala
XM_005265653.4:c.1256G>C	XP_005265710.1:p.Gly419Ala
XM_011531735.3:c.1412G>C	XP_011530037.1:p.Gly471Ala
XM_017007878.2:c.1412G>C	XP_016863367.1:p.Gly471Ala
XM_017007879.2:c.1409G>C	XP_016863368.1:p.Gly470Ala
XM_017007880.2:c.1256G>C	XP_016863369.1:p.Gly419Ala
XM_017007881.2:c.1253G>C	XP_016863370.1:p.Gly418Ala
NM_001281767.3:c.1748G>C	NP_001268696.1:p.Gly583Ala
NM_004439.8:c.1745G>C	NP_004430.4:p.Gly582Ala
NM_182472.5:c.1745G>C	NP_872272.2:p.Gly582Ala
NM_001281765.3:c.1748G>C	NP_001268694.1:p.Gly583Ala
NM_001281766.3:c.1748G>C MANE Select	NP_001268695.1:p.Gly583Ala
NM_001318761.2:c.1541G>C	NP_001305690.1:p.Gly514Ala