Canonical Allele Identifier: CA379597240

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163512G>A (hg19) ; chr11:g.9141965G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141965G>A , CM000673.2:g.9141965G>A	GRCh38
NC_000011.9:g.9163512G>A , CM000673.1:g.9163512G>A	GRCh37
NC_000011.8:g.9120088G>A	NCBI36
NG_053019.1:g.128371C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3655C>T MANE Select	ENSP00000328524.3:p.Gln1219Ter
ENST00000525784.6:n.1517C>T
ENST00000530780.2:c.*3481C>T	ENSP00000433925.1:n.*3481C>T
ENST00000531747.2:n.3326C>T
ENST00000679446.1:n.3576C>T
ENST00000679458.1:n.5056C>T
ENST00000679460.1:n.4717C>T
ENST00000679568.1:c.3655C>T	ENSP00000505860.1:p.Gln1219Ter
ENST00000679745.1:n.4160C>T
ENST00000679773.1:n.2816C>T
ENST00000679926.1:n.4957C>T
ENST00000679999.1:c.*712C>T	ENSP00000505198.1:n.*712C>T
ENST00000680252.1:c.3322C>T
ENST00000680294.1:c.3448C>T	ENSP00000506113.1:p.Gln1150Ter
ENST00000680358.1:n.2954C>T
ENST00000680470.1:c.*1436C>T	ENSP00000505975.1:n.*1436C>T
ENST00000680554.1:c.*188C>T	ENSP00000505621.1:n.*188C>T
ENST00000680576.1:n.5131C>T
ENST00000680599.1:n.3696C>T
ENST00000680742.1:c.*179+9C>T	ENSP00000505206.1:n.*179+9C>T
ENST00000680791.1:n.2539C>T
ENST00000680885.1:n.5357C>T
ENST00000681158.1:c.3239C>T
ENST00000681203.1:c.3583C>T	ENSP00000506456.1:p.Gln1195Ter
ENST00000681371.1:n.3527C>T
ENST00000681425.1:n.4133C>T
ENST00000681639.1:n.1934C>T
ENST00000328194.7:c.3655C>T	ENSP00000328524.3:p.Gln1219Ter
ENST00000525784.5:c.591C>T
ENST00000527700.5:n.3217C>T
ENST00000528725.5:c.351C>T
ENST00000529977.5:n.1556C>T
ENST00000530044.5:c.3646+9C>T	ENSP00000435866.1:n.3646+9C>T
ENST00000531747.1:c.891C>T
ENST00000533737.5:c.318C>T
NM_001243254.1:c.3646+9C>T	NP_001230183.1:n.3646+9C>T
NM_015213.3:c.3655C>T	NP_056028.2:p.Gln1219Ter
XM_005252832.1:c.3655C>T	XP_005252889.1:p.Gln1219Ter
XM_011519952.1:c.3646+9C>T	XP_011518254.1:n.3646+9C>T
XM_011519953.1:c.1753C>T	XP_011518255.1:p.Gln585Ter
XR_242782.2:n.3837C>T
XR_930851.1:n.3828+9C>T
NM_001348749.1:c.3583C>T	NP_001335678.1:p.Gln1195Ter
NM_001348750.1:c.3367C>T	NP_001335679.1:p.Gln1123Ter
NR_145966.2:n.3829C>T
NM_015213.4:c.3655C>T MANE Select	NP_056028.2:p.Gln1219Ter
NM_001243254.2:c.3646+9C>T	NP_001230183.1:n.3646+9C>T
NM_001348749.2:c.3583C>T	NP_001335678.1:p.Gln1195Ter
NM_001348750.2:c.3367C>T	NP_001335679.1:p.Gln1123Ter