Canonical Allele Identifier: CA379598239

Gene: DENND5A

Linked Data

• dbSNP Id: rs1554909152
• MyVariant Identifiers: chr11:g.9163647G>A (hg19) ; chr11:g.9142100G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142100G>A , CM000673.2:g.9142100G>A	GRCh38
NC_000011.9:g.9163647G>A , CM000673.1:g.9163647G>A	GRCh37
NC_000011.8:g.9120223G>A	NCBI36
NG_053019.1:g.128236C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3520C>T MANE Select	ENSP00000328524.3:p.Gln1174Ter
ENST00000525784.6:n.1382C>T
ENST00000530780.2:c.*3346C>T	ENSP00000433925.1:n.*3346C>T
ENST00000531747.2:n.3191C>T
ENST00000679446.1:n.3441C>T
ENST00000679458.1:n.4921C>T
ENST00000679460.1:n.4582C>T
ENST00000679568.1:c.3520C>T	ENSP00000505860.1:p.Gln1174Ter
ENST00000679745.1:n.4025C>T
ENST00000679773.1:n.2681C>T
ENST00000679926.1:n.4822C>T
ENST00000679999.1:c.*577C>T	ENSP00000505198.1:n.*577C>T
ENST00000680252.1:c.3187C>T
ENST00000680294.1:c.3313C>T	ENSP00000506113.1:p.Gln1105Ter
ENST00000680358.1:n.2819C>T
ENST00000680470.1:c.*1301C>T	ENSP00000505975.1:n.*1301C>T
ENST00000680554.1:c.*53C>T	ENSP00000505621.1:n.*53C>T
ENST00000680576.1:n.4996C>T
ENST00000680599.1:n.3561C>T
ENST00000680742.1:c.*53C>T	ENSP00000505206.1:n.*53C>T
ENST00000680791.1:n.2404C>T
ENST00000680885.1:n.5222C>T
ENST00000681158.1:c.3104C>T
ENST00000681203.1:c.3448C>T	ENSP00000506456.1:p.Gln1150Ter
ENST00000681371.1:n.3392C>T
ENST00000681425.1:n.3998C>T
ENST00000681639.1:n.1799C>T
ENST00000328194.7:c.3520C>T	ENSP00000328524.3:p.Gln1174Ter
ENST00000525784.5:c.456C>T
ENST00000527700.5:n.3082C>T
ENST00000528725.5:c.216C>T
ENST00000529977.5:n.1421C>T
ENST00000530044.5:c.3520C>T	ENSP00000435866.1:p.Gln1174Ter
ENST00000531747.1:c.756C>T
ENST00000533737.5:c.183C>T
NM_001243254.1:c.3520C>T	NP_001230183.1:p.Gln1174Ter
NM_015213.3:c.3520C>T	NP_056028.2:p.Gln1174Ter
XM_005252832.1:c.3520C>T	XP_005252889.1:p.Gln1174Ter
XM_011519952.1:c.3520C>T	XP_011518254.1:p.Gln1174Ter
XM_011519953.1:c.1618C>T	XP_011518255.1:p.Gln540Ter
XR_242782.2:n.3702C>T
XR_930851.1:n.3702C>T
NM_001348749.1:c.3448C>T	NP_001335678.1:p.Gln1150Ter
NM_001348750.1:c.3232C>T	NP_001335679.1:p.Gln1078Ter
NR_145966.2:n.3694C>T
NM_015213.4:c.3520C>T MANE Select	NP_056028.2:p.Gln1174Ter
NM_001243254.2:c.3520C>T	NP_001230183.1:p.Gln1174Ter
NM_001348749.2:c.3448C>T	NP_001335678.1:p.Gln1150Ter
NM_001348750.2:c.3232C>T	NP_001335679.1:p.Gln1078Ter