Canonical Allele Identifier: CA379598102

Gene: DENND5A

Linked Data

• dbSNP Id: rs1554909133
• MyVariant Identifiers: chr11:g.9163623T>A (hg19) ; chr11:g.9142076T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142076T>A , CM000673.2:g.9142076T>A	GRCh38
NC_000011.9:g.9163623T>A , CM000673.1:g.9163623T>A	GRCh37
NC_000011.8:g.9120199T>A	NCBI36
NG_053019.1:g.128260A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3544A>T MANE Select	ENSP00000328524.3:p.Lys1182Ter
ENST00000525784.6:n.1406A>T
ENST00000530780.2:c.*3370A>T	ENSP00000433925.1:n.*3370A>T
ENST00000531747.2:n.3215A>T
ENST00000679446.1:n.3465A>T
ENST00000679458.1:n.4945A>T
ENST00000679460.1:n.4606A>T
ENST00000679568.1:c.3544A>T	ENSP00000505860.1:p.Lys1182Ter
ENST00000679745.1:n.4049A>T
ENST00000679773.1:n.2705A>T
ENST00000679926.1:n.4846A>T
ENST00000679999.1:c.*601A>T	ENSP00000505198.1:n.*601A>T
ENST00000680252.1:c.3211A>T
ENST00000680294.1:c.3337A>T	ENSP00000506113.1:p.Lys1113Ter
ENST00000680358.1:n.2843A>T
ENST00000680470.1:c.*1325A>T	ENSP00000505975.1:n.*1325A>T
ENST00000680554.1:c.*77A>T	ENSP00000505621.1:n.*77A>T
ENST00000680576.1:n.5020A>T
ENST00000680599.1:n.3585A>T
ENST00000680742.1:c.*77A>T	ENSP00000505206.1:n.*77A>T
ENST00000680791.1:n.2428A>T
ENST00000680885.1:n.5246A>T
ENST00000681158.1:c.3128A>T
ENST00000681203.1:c.3472A>T	ENSP00000506456.1:p.Lys1158Ter
ENST00000681371.1:n.3416A>T
ENST00000681425.1:n.4022A>T
ENST00000681639.1:n.1823A>T
ENST00000328194.7:c.3544A>T	ENSP00000328524.3:p.Lys1182Ter
ENST00000525784.5:c.480A>T
ENST00000527700.5:n.3106A>T
ENST00000528725.5:c.240A>T
ENST00000529977.5:n.1445A>T
ENST00000530044.5:c.3544A>T	ENSP00000435866.1:p.Lys1182Ter
ENST00000531747.1:c.780A>T
ENST00000533737.5:c.207A>T
NM_001243254.1:c.3544A>T	NP_001230183.1:p.Lys1182Ter
NM_015213.3:c.3544A>T	NP_056028.2:p.Lys1182Ter
XM_005252832.1:c.3544A>T	XP_005252889.1:p.Lys1182Ter
XM_011519952.1:c.3544A>T	XP_011518254.1:p.Lys1182Ter
XM_011519953.1:c.1642A>T	XP_011518255.1:p.Lys548Ter
XR_242782.2:n.3726A>T
XR_930851.1:n.3726A>T
NM_001348749.1:c.3472A>T	NP_001335678.1:p.Lys1158Ter
NM_001348750.1:c.3256A>T	NP_001335679.1:p.Lys1086Ter
NR_145966.2:n.3718A>T
NM_015213.4:c.3544A>T MANE Select	NP_056028.2:p.Lys1182Ter
NM_001243254.2:c.3544A>T	NP_001230183.1:p.Lys1182Ter
NM_001348749.2:c.3472A>T	NP_001335678.1:p.Lys1158Ter
NM_001348750.2:c.3256A>T	NP_001335679.1:p.Lys1086Ter