Canonical Allele Identifier: CA379597595

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163550T>G (hg19) ; chr11:g.9142003T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142003T>G , CM000673.2:g.9142003T>G	GRCh38
NC_000011.9:g.9163550T>G , CM000673.1:g.9163550T>G	GRCh37
NC_000011.8:g.9120126T>G	NCBI36
NG_053019.1:g.128333A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000328194.8:c.3617A>C MANE Select	ENSP00000328524.3:p.Asn1206Thr
ENST00000525784.6:n.1479A>C
ENST00000530780.2:c.*3443A>C	ENSP00000433925.1:n.*3443A>C
ENST00000531747.2:n.3288A>C
ENST00000679446.1:n.3538A>C
ENST00000679458.1:n.5018A>C
ENST00000679460.1:n.4679A>C
ENST00000679568.1:c.3617A>C	ENSP00000505860.1:p.Asn1206Thr
ENST00000679745.1:n.4122A>C
ENST00000679773.1:n.2778A>C
ENST00000679926.1:n.4919A>C
ENST00000679999.1:c.*674A>C	ENSP00000505198.1:n.*674A>C
ENST00000680252.1:c.3284A>C
ENST00000680294.1:c.3410A>C	ENSP00000506113.1:p.Asn1137Thr
ENST00000680358.1:n.2916A>C
ENST00000680470.1:c.*1398A>C	ENSP00000505975.1:n.*1398A>C
ENST00000680554.1:c.*150A>C	ENSP00000505621.1:n.*150A>C
ENST00000680576.1:n.5093A>C
ENST00000680599.1:n.3658A>C
ENST00000680742.1:c.*150A>C	ENSP00000505206.1:n.*150A>C
ENST00000680791.1:n.2501A>C
ENST00000680885.1:n.5319A>C
ENST00000681158.1:c.3201A>C
ENST00000681203.1:c.3545A>C	ENSP00000506456.1:p.Asn1182Thr
ENST00000681371.1:n.3489A>C
ENST00000681425.1:n.4095A>C
ENST00000681639.1:n.1896A>C
ENST00000328194.7:c.3617A>C	ENSP00000328524.3:p.Asn1206Thr
ENST00000525784.5:c.553A>C
ENST00000527700.5:n.3179A>C
ENST00000528725.5:c.313A>C
ENST00000529977.5:n.1518A>C
ENST00000530044.5:c.3617A>C	ENSP00000435866.1:p.Asn1206Thr
ENST00000531747.1:c.853A>C
ENST00000533737.5:c.280A>C
NM_001243254.1:c.3617A>C	NP_001230183.1:p.Asn1206Thr
NM_015213.3:c.3617A>C	NP_056028.2:p.Asn1206Thr
XM_005252832.1:c.3617A>C	XP_005252889.1:p.Asn1206Thr
XM_011519952.1:c.3617A>C	XP_011518254.1:p.Asn1206Thr
XM_011519953.1:c.1715A>C	XP_011518255.1:p.Asn572Thr
XR_242782.2:n.3799A>C
XR_930851.1:n.3799A>C
NM_001348749.1:c.3545A>C	NP_001335678.1:p.Asn1182Thr
NM_001348750.1:c.3329A>C	NP_001335679.1:p.Asn1110Thr
NR_145966.2:n.3791A>C
NM_015213.4:c.3617A>C MANE Select	NP_056028.2:p.Asn1206Thr
NM_001243254.2:c.3617A>C	NP_001230183.1:p.Asn1206Thr
NM_001348749.2:c.3545A>C	NP_001335678.1:p.Asn1182Thr
NM_001348750.2:c.3329A>C	NP_001335679.1:p.Asn1110Thr