Canonical Allele Identifier: CA379598087

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163620T>C (hg19) ; chr11:g.9142073T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142073T>C , CM000673.2:g.9142073T>C	GRCh38
NC_000011.9:g.9163620T>C , CM000673.1:g.9163620T>C	GRCh37
NC_000011.8:g.9120196T>C	NCBI36
NG_053019.1:g.128263A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3547A>G MANE Select	ENSP00000328524.3:p.Asn1183Asp
ENST00000525784.6:n.1409A>G
ENST00000530780.2:c.*3373A>G	ENSP00000433925.1:n.*3373A>G
ENST00000531747.2:n.3218A>G
ENST00000679446.1:n.3468A>G
ENST00000679458.1:n.4948A>G
ENST00000679460.1:n.4609A>G
ENST00000679568.1:c.3547A>G	ENSP00000505860.1:p.Asn1183Asp
ENST00000679745.1:n.4052A>G
ENST00000679773.1:n.2708A>G
ENST00000679926.1:n.4849A>G
ENST00000679999.1:c.*604A>G	ENSP00000505198.1:n.*604A>G
ENST00000680252.1:c.3214A>G
ENST00000680294.1:c.3340A>G	ENSP00000506113.1:p.Asn1114Asp
ENST00000680358.1:n.2846A>G
ENST00000680470.1:c.*1328A>G	ENSP00000505975.1:n.*1328A>G
ENST00000680554.1:c.*80A>G	ENSP00000505621.1:n.*80A>G
ENST00000680576.1:n.5023A>G
ENST00000680599.1:n.3588A>G
ENST00000680742.1:c.*80A>G	ENSP00000505206.1:n.*80A>G
ENST00000680791.1:n.2431A>G
ENST00000680885.1:n.5249A>G
ENST00000681158.1:c.3131A>G
ENST00000681203.1:c.3475A>G	ENSP00000506456.1:p.Asn1159Asp
ENST00000681371.1:n.3419A>G
ENST00000681425.1:n.4025A>G
ENST00000681639.1:n.1826A>G
ENST00000328194.7:c.3547A>G	ENSP00000328524.3:p.Asn1183Asp
ENST00000525784.5:c.483A>G
ENST00000527700.5:n.3109A>G
ENST00000528725.5:c.243A>G
ENST00000529977.5:n.1448A>G
ENST00000530044.5:c.3547A>G	ENSP00000435866.1:p.Asn1183Asp
ENST00000531747.1:c.783A>G
ENST00000533737.5:c.210A>G
NM_001243254.1:c.3547A>G	NP_001230183.1:p.Asn1183Asp
NM_015213.3:c.3547A>G	NP_056028.2:p.Asn1183Asp
XM_005252832.1:c.3547A>G	XP_005252889.1:p.Asn1183Asp
XM_011519952.1:c.3547A>G	XP_011518254.1:p.Asn1183Asp
XM_011519953.1:c.1645A>G	XP_011518255.1:p.Asn549Asp
XR_242782.2:n.3729A>G
XR_930851.1:n.3729A>G
NM_001348749.1:c.3475A>G	NP_001335678.1:p.Asn1159Asp
NM_001348750.1:c.3259A>G	NP_001335679.1:p.Asn1087Asp
NR_145966.2:n.3721A>G
NM_015213.4:c.3547A>G MANE Select	NP_056028.2:p.Asn1183Asp
NM_001243254.2:c.3547A>G	NP_001230183.1:p.Asn1183Asp
NM_001348749.2:c.3475A>G	NP_001335678.1:p.Asn1159Asp
NM_001348750.2:c.3259A>G	NP_001335679.1:p.Asn1087Asp