Canonical Allele Identifier: CA8592486

Gene: ETV4 DHX8

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43545372G>T , CM000679.2:g.43545372G>T	GRCh38
NC_000017.10:g.41622740G>T , CM000679.1:g.41622740G>T	GRCh37
NC_000017.9:g.38978266G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001079675.5:c.61-5C>A (ETV4) MANE Select	NP_001073143.1:n.61-5C>A
ENST00000319349.10:c.61-5C>A (ETV4) MANE Select	ENSP00000321835.4:n.61-5C>A
NM_001079675.2:c.61-5C>A (ETV4)	NP_001073143.1:n.61-5C>A
NM_001079675.3:c.61-5C>A (ETV4)	NP_001073143.1:n.61-5C>A
NM_001261437.1:c.-57-5C>A (ETV4)	NP_001248366.1:n.-57-5C>A
NM_001261437.3:c.-57-5C>A (ETV4)	NP_001248366.1:n.-57-5C>A
NM_001261438.1:c.-57-5C>A (ETV4)	NP_001248367.1:n.-57-5C>A
NM_001261438.3:c.-57-5C>A (ETV4)	NP_001248367.1:n.-57-5C>A
NM_001369366.2:c.61-5C>A (ETV4)	NP_001356295.1:n.61-5C>A
NM_001369367.2:c.61-5C>A (ETV4)	NP_001356296.1:n.61-5C>A
NM_001369368.2:c.61-5C>A (ETV4)	NP_001356297.1:n.61-5C>A
NM_001986.2:c.61-5C>A (ETV4)	NP_001977.1:n.61-5C>A
NM_001986.4:c.61-5C>A (ETV4)	NP_001977.1:n.61-5C>A
ENST00000319349.9:c.61-5C>A (ETV4)	ENSP00000321835.4:n.61-5C>A
ENST00000393664.6:c.61-5C>A (ETV4)	ENSP00000377273.1:n.61-5C>A
ENST00000538265.5:c.-57-5C>A (ETV4)	ENSP00000443846.1:n.-57-5C>A
ENST00000545089.5:c.61-5C>A (ETV4)	ENSP00000441749.1:n.61-5C>A
ENST00000545954.5:c.-57-5C>A (ETV4)	ENSP00000440023.1:n.-57-5C>A
ENST00000585508.5:n.428C>A (ETV4)
ENST00000586764.1:c.-57-5C>A (ETV4)	ENSP00000466673.1:n.-57-5C>A
ENST00000587151.5:n.277-5C>A (ETV4)
ENST00000588996.1:n.31+557G>T
ENST00000590236.5:n.31C>A (ETV4)
ENST00000591713.5:c.61-5C>A (ETV4)	ENSP00000465718.1:n.61-5C>A
ENST00000650571.1:c.*425+8874G>T (DHX8)	ENSP00000496923.1:n.*425+8874G>T
XM_011524511.1:c.61-2C>A (ETV4)	XP_011522813.1:n.61-2C>A
XM_011524512.1:c.61-2C>A (ETV4)	XP_011522814.1:n.61-2C>A
XM_011524513.1:c.61-2C>A (ETV4)	XP_011522815.1:n.61-2C>A
XM_017024349.1:c.61-5C>A (ETV4)	XP_016879838.1:n.61-5C>A
XM_024450644.1:c.-463-5C>A (ETV4)	XP_024306412.1:n.-463-5C>A