Canonical Allele Identifier: CA379597203

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163507C>T (hg19) ; chr11:g.9141960C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141960C>T , CM000673.2:g.9141960C>T	GRCh38
NC_000011.9:g.9163507C>T , CM000673.1:g.9163507C>T	GRCh37
NC_000011.8:g.9120083C>T	NCBI36
NG_053019.1:g.128376G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3660G>A MANE Select	ENSP00000328524.3:p.Met1220Ile
ENST00000525784.6:n.1522G>A
ENST00000530780.2:c.*3486G>A	ENSP00000433925.1:n.*3486G>A
ENST00000531747.2:n.3331G>A
ENST00000679446.1:n.3581G>A
ENST00000679458.1:n.5061G>A
ENST00000679460.1:n.4722G>A
ENST00000679568.1:c.3660G>A	ENSP00000505860.1:p.Met1220Ile
ENST00000679745.1:n.4165G>A
ENST00000679773.1:n.2821G>A
ENST00000679926.1:n.4962G>A
ENST00000679999.1:c.*717G>A	ENSP00000505198.1:n.*717G>A
ENST00000680252.1:c.3327G>A
ENST00000680294.1:c.3453G>A	ENSP00000506113.1:p.Met1151Ile
ENST00000680358.1:n.2959G>A
ENST00000680470.1:c.*1441G>A	ENSP00000505975.1:n.*1441G>A
ENST00000680554.1:c.*193G>A	ENSP00000505621.1:n.*193G>A
ENST00000680576.1:n.5136G>A
ENST00000680599.1:n.3701G>A
ENST00000680742.1:c.*179+14G>A	ENSP00000505206.1:n.*179+14G>A
ENST00000680791.1:n.2544G>A
ENST00000680885.1:n.5362G>A
ENST00000681158.1:c.3244G>A
ENST00000681203.1:c.3588G>A	ENSP00000506456.1:p.Met1196Ile
ENST00000681371.1:n.3532G>A
ENST00000681425.1:n.4138G>A
ENST00000681639.1:n.1939G>A
ENST00000328194.7:c.3660G>A	ENSP00000328524.3:p.Met1220Ile
ENST00000525784.5:c.596G>A
ENST00000527700.5:n.3222G>A
ENST00000528725.5:c.356G>A
ENST00000529977.5:n.1561G>A
ENST00000530044.5:c.3646+14G>A	ENSP00000435866.1:n.3646+14G>A
ENST00000531747.1:c.896G>A
ENST00000533737.5:c.323G>A
NM_001243254.1:c.3646+14G>A	NP_001230183.1:n.3646+14G>A
NM_015213.3:c.3660G>A	NP_056028.2:p.Met1220Ile
XM_005252832.1:c.3660G>A	XP_005252889.1:p.Met1220Ile
XM_011519952.1:c.3646+14G>A	XP_011518254.1:n.3646+14G>A
XM_011519953.1:c.1758G>A	XP_011518255.1:p.Met586Ile
XR_242782.2:n.3842G>A
XR_930851.1:n.3828+14G>A
NM_001348749.1:c.3588G>A	NP_001335678.1:p.Met1196Ile
NM_001348750.1:c.3372G>A	NP_001335679.1:p.Met1124Ile
NR_145966.2:n.3834G>A
NM_015213.4:c.3660G>A MANE Select	NP_056028.2:p.Met1220Ile
NM_001243254.2:c.3646+14G>A	NP_001230183.1:n.3646+14G>A
NM_001348749.2:c.3588G>A	NP_001335678.1:p.Met1196Ile
NM_001348750.2:c.3372G>A	NP_001335679.1:p.Met1124Ile