Canonical Allele Identifier: CA2580083866

Gene: DEAF1 EPS8L2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.694970_694984del , CM000673.2:g.694970_694984del	GRCh38
NC_000011.9:g.694970_694984del , CM000673.1:g.694970_694984del	GRCh37
NC_000011.8:g.684970_684984del	NCBI36
NG_034156.1:g.5776_5790del
NG_034156.2:g.17105_17119del

Transcript Alleles

HGVS	Amino-acid Change
NM_021008.4:c.69_83del (DEAF1) MANE Select	NP_066288.2:p.Ala24_Ala28del
ENST00000382409.4:c.69_83del (DEAF1) MANE Select	ENSP00000371846.3:p.Ala24_Ala28del
NM_001293634.1:c.69_83del (DEAF1)	NP_001280563.1:p.Ala24_Ala28del
NM_001367390.1:c.-437-3381_-437-3367del (DEAF1)	NP_001354319.1:n.-437-3381_-437-3367del
NM_021008.3:c.69_83del (DEAF1)	NP_066288.2:p.Ala24_Ala28del
ENST00000382409.3:c.69_83del (DEAF1)	ENSP00000371846.3:p.Ala24_Ala28del
ENST00000524763.5:c.-227+495_-227+509del (EPS8L2)	ENSP00000435128.1:n.-227+495_-227+509del
ENST00000525626.5:n.145-3381_145-3367del (DEAF1)
ENST00000683307.1:c.-437-3381_-437-3367del (DEAF1)	ENSP00000507198.1:n.-437-3381_-437-3367del
ENST00000685854.1:c.-136_-122del (DEAF1)	ENSP00000508801.1:n.-136_-122del
ENST00000686001.1:c.-136_-122del (DEAF1)	ENSP00000508459.1:n.-136_-122del
ENST00000687329.1:c.-136_-122del (DEAF1)	ENSP00000510598.1:n.-136_-122del
ENST00000689835.1:c.-136_-122del (DEAF1)	ENSP00000510621.1:n.-136_-122del
ENST00000690068.1:c.-136_-122del (DEAF1)	ENSP00000509089.1:n.-136_-122del
ENST00000692634.1:c.-136_-122del (DEAF1)	ENSP00000508859.1:n.-136_-122del
ENST00000693164.1:n.63_77del (DEAF1)
XM_011519842.1:c.69_83del (DEAF1)	XP_011518144.1:p.Ala24_Ala28del
XM_011519842.3:c.69_83del (DEAF1)	XP_011518144.1:p.Ala24_Ala28del
XM_011519843.1:c.69_83del (DEAF1)	XP_011518145.1:p.Ala24_Ala28del
XM_024448325.1:c.69_83del (DEAF1)	XP_024304093.1:p.Ala24_Ala28del
XM_024448326.1:c.69_83del (DEAF1)	XP_024304094.1:p.Ala24_Ala28del
XM_024448327.1:c.69_83del (DEAF1)	XP_024304095.1:p.Ala24_Ala28del
XR_428838.2:n.75_89del (DEAF1)
XR_930843.1:n.75_89del (DEAF1)