Canonical Allele Identifier: CA378932087

Gene: DEAF1

Linked Data

• MyVariant Identifiers: chr11:g.686901C>G (hg19) ; chr11:g.686901C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.686901C>G , CM000673.2:g.686901C>G	GRCh38
NC_000011.9:g.686901C>G , CM000673.1:g.686901C>G	GRCh37
NC_000011.8:g.676901C>G	NCBI36
NG_034156.1:g.13854G>C
NG_034156.2:g.25183G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000525626.6:n.646G>C
ENST00000528864.6:n.647G>C
ENST00000530813.2:c.*384G>C	ENSP00000508507.1:n.*384G>C
ENST00000682936.1:n.521G>C
ENST00000683307.1:c.35G>C	ENSP00000507198.1:p.Arg12Thr
ENST00000684249.1:n.949G>C
ENST00000685854.1:c.557G>C	ENSP00000508801.1:p.Arg186Thr
ENST00000686001.1:c.557G>C	ENSP00000508459.1:p.Arg186Thr
ENST00000687329.1:c.557G>C	ENSP00000510598.1:p.Arg186Thr
ENST00000689835.1:c.557G>C	ENSP00000510621.1:p.Arg186Thr
ENST00000690068.1:c.557G>C	ENSP00000509089.1:p.Arg186Thr
ENST00000692634.1:c.557G>C	ENSP00000508859.1:p.Arg186Thr
ENST00000693164.1:n.755G>C
ENST00000382409.4:c.761G>C MANE Select	ENSP00000371846.3:p.Arg254Thr
ENST00000382409.3:c.761G>C	ENSP00000371846.3:p.Arg254Thr
ENST00000527170.5:c.123G>C
NM_001293634.1:c.664+1010G>C	NP_001280563.1:n.664+1010G>C
NM_021008.3:c.761G>C	NP_066288.2:p.Arg254Thr
XM_011519842.1:c.761G>C	XP_011518144.1:p.Arg254Thr
XM_011519843.1:c.761G>C	XP_011518145.1:p.Arg254Thr
XR_428838.2:n.767G>C
XR_930843.1:n.767G>C
XM_011519842.3:c.761G>C	XP_011518144.1:p.Arg254Thr
XM_024448325.1:c.761G>C	XP_024304093.1:p.Arg254Thr
XM_024448326.1:c.761G>C	XP_024304094.1:p.Arg254Thr
XM_024448327.1:c.761G>C	XP_024304095.1:p.Arg254Thr
NM_001367390.1:c.35G>C	NP_001354319.1:p.Arg12Thr
NM_021008.4:c.761G>C MANE Select	NP_066288.2:p.Arg254Thr