Canonical Allele Identifier: CA378931835

Gene: DEAF1

Linked Data

• ClinVar Variation Id: 2098659
• ClinVar RCV Id: RCV003031057
• MyVariant Identifiers: chr11:g.686874A>G (hg19) ; chr11:g.686874A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.686874A>G , CM000673.2:g.686874A>G	GRCh38
NC_000011.9:g.686874A>G , CM000673.1:g.686874A>G	GRCh37
NC_000011.8:g.676874A>G	NCBI36
NG_034156.1:g.13881T>C
NG_034156.2:g.25210T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000525626.6:n.673T>C
ENST00000528864.6:n.674T>C
ENST00000530813.2:c.*411T>C	ENSP00000508507.1:n.*411T>C
ENST00000682936.1:n.548T>C
ENST00000683307.1:c.62T>C	ENSP00000507198.1:p.Leu21Ser
ENST00000684249.1:n.976T>C
ENST00000685854.1:c.584T>C	ENSP00000508801.1:p.Leu195Ser
ENST00000686001.1:c.584T>C	ENSP00000508459.1:p.Leu195Ser
ENST00000687329.1:c.584T>C	ENSP00000510598.1:p.Leu195Ser
ENST00000689835.1:c.584T>C	ENSP00000510621.1:p.Leu195Ser
ENST00000690068.1:c.584T>C	ENSP00000509089.1:p.Leu195Ser
ENST00000692634.1:c.584T>C	ENSP00000508859.1:p.Leu195Ser
ENST00000693164.1:n.782T>C
ENST00000382409.4:c.788T>C MANE Select	ENSP00000371846.3:p.Leu263Ser
ENST00000382409.3:c.788T>C	ENSP00000371846.3:p.Leu263Ser
ENST00000527170.5:c.150T>C
NM_001293634.1:c.664+1037T>C	NP_001280563.1:n.664+1037T>C
NM_021008.3:c.788T>C	NP_066288.2:p.Leu263Ser
XM_011519842.1:c.788T>C	XP_011518144.1:p.Leu263Ser
XM_011519843.1:c.788T>C	XP_011518145.1:p.Leu263Ser
XR_428838.2:n.794T>C
XR_930843.1:n.794T>C
XM_011519842.3:c.788T>C	XP_011518144.1:p.Leu263Ser
XM_024448325.1:c.788T>C	XP_024304093.1:p.Leu263Ser
XM_024448326.1:c.788T>C	XP_024304094.1:p.Leu263Ser
XM_024448327.1:c.788T>C	XP_024304095.1:p.Leu263Ser
NM_001367390.1:c.62T>C	NP_001354319.1:p.Leu21Ser
NM_021008.4:c.788T>C MANE Select	NP_066288.2:p.Leu263Ser