Canonical Allele Identifier: CA2582341854

Gene: DEAF1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.679792_679798delinsCCCA , CM000673.2:g.679792_679798delinsCCCA	GRCh38
NC_000011.9:g.679792_679798delinsCCCA , CM000673.1:g.679792_679798delinsCCCA	GRCh37
NC_000011.8:g.669792_669798delinsCCCA	NCBI36
NG_034156.1:g.20957_20963delinsTGGG
NG_034156.2:g.32286_32292delinsTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525626.6:n.901_907delinsTGGG
ENST00000528864.6:n.902_908delinsTGGG
ENST00000530813.2:c.*639_*645delinsTGGG	ENSP00000508507.1:n.*639_*645delinsTGGG
ENST00000682936.1:n.776_782delinsTGGG
ENST00000683307.1:c.290_296delinsTGGG	ENSP00000507198.1:p.Gly97_Ile99delinsValGly
ENST00000685854.1:c.812_818delinsTGGG	ENSP00000508801.1:p.Gly271_Ile273delinsValGly
ENST00000686001.1:c.812_818delinsTGGG	ENSP00000508459.1:p.Gly271_Ile273delinsValGly
ENST00000687329.1:c.812_818delinsTGGG	ENSP00000510598.1:p.Gly271_Ile273delinsValGly
ENST00000689835.1:c.812_818delinsTGGG	ENSP00000510621.1:p.Gly271_Ile273delinsValGly
ENST00000690068.1:c.812_818delinsTGGG	ENSP00000509089.1:p.Gly271_Ile273delinsValGly
ENST00000692634.1:c.667-976_667-970delinsTGGG	ENSP00000508859.1:n.667-976_667-970delinsTGGG
ENST00000382409.4:c.1016_1022delinsTGGG MANE Select	ENSP00000371846.3:p.Gly339_Ile341delinsValGly
ENST00000382409.3:c.1016_1022delinsTGGG	ENSP00000371846.3:p.Gly339_Ile341delinsValGly
ENST00000525904.5:n.199_205delinsTGGG
ENST00000527170.5:c.378_384delinsTGGG
ENST00000530813.1:n.220_226delinsTGGG
NM_001293634.1:c.749_755delinsTGGG	NP_001280563.1:p.Gly250_Ile252delinsValGly
NM_021008.3:c.1016_1022delinsTGGG	NP_066288.2:p.Gly339_Ile341delinsValGly
XM_011519842.1:c.1016_1022delinsTGGG	XP_011518144.1:p.Gly339_Ile341delinsValGly
XM_011519843.1:c.1016_1022delinsTGGG	XP_011518145.1:p.Gly339_Ile341delinsValGly
XR_428838.2:n.1022_1028delinsTGGG
XR_930843.1:n.1022_1028delinsTGGG
XM_011519842.3:c.1016_1022delinsTGGG	XP_011518144.1:p.Gly339_Ile341delinsValGly
XM_024448325.1:c.1016_1022delinsTGGG	XP_024304093.1:p.Gly339_Ile341delinsValGly
XM_024448326.1:c.1016_1022delinsTGGG	XP_024304094.1:p.Gly339_Ile341delinsValGly
XM_024448327.1:c.1016_1022delinsTGGG	XP_024304095.1:p.Gly339_Ile341delinsValGly
NM_001367390.1:c.290_296delinsTGGG	NP_001354319.1:p.Gly97_Ile99delinsValGly
NM_021008.4:c.1016_1022delinsTGGG MANE Select	NP_066288.2:p.Gly339_Ile341delinsValGly