Canonical Allele Identifier: CA379597570

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163547T>G (hg19) ; chr11:g.9142000T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142000T>G , CM000673.2:g.9142000T>G	GRCh38
NC_000011.9:g.9163547T>G , CM000673.1:g.9163547T>G	GRCh37
NC_000011.8:g.9120123T>G	NCBI36
NG_053019.1:g.128336A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000328194.8:c.3620A>C MANE Select	ENSP00000328524.3:p.Asn1207Thr
ENST00000525784.6:n.1482A>C
ENST00000530780.2:c.*3446A>C	ENSP00000433925.1:n.*3446A>C
ENST00000531747.2:n.3291A>C
ENST00000679446.1:n.3541A>C
ENST00000679458.1:n.5021A>C
ENST00000679460.1:n.4682A>C
ENST00000679568.1:c.3620A>C	ENSP00000505860.1:p.Asn1207Thr
ENST00000679745.1:n.4125A>C
ENST00000679773.1:n.2781A>C
ENST00000679926.1:n.4922A>C
ENST00000679999.1:c.*677A>C	ENSP00000505198.1:n.*677A>C
ENST00000680252.1:c.3287A>C
ENST00000680294.1:c.3413A>C	ENSP00000506113.1:p.Asn1138Thr
ENST00000680358.1:n.2919A>C
ENST00000680470.1:c.*1401A>C	ENSP00000505975.1:n.*1401A>C
ENST00000680554.1:c.*153A>C	ENSP00000505621.1:n.*153A>C
ENST00000680576.1:n.5096A>C
ENST00000680599.1:n.3661A>C
ENST00000680742.1:c.*153A>C	ENSP00000505206.1:n.*153A>C
ENST00000680791.1:n.2504A>C
ENST00000680885.1:n.5322A>C
ENST00000681158.1:c.3204A>C
ENST00000681203.1:c.3548A>C	ENSP00000506456.1:p.Asn1183Thr
ENST00000681371.1:n.3492A>C
ENST00000681425.1:n.4098A>C
ENST00000681639.1:n.1899A>C
ENST00000328194.7:c.3620A>C	ENSP00000328524.3:p.Asn1207Thr
ENST00000525784.5:c.556A>C
ENST00000527700.5:n.3182A>C
ENST00000528725.5:c.316A>C
ENST00000529977.5:n.1521A>C
ENST00000530044.5:c.3620A>C	ENSP00000435866.1:p.Asn1207Thr
ENST00000531747.1:c.856A>C
ENST00000533737.5:c.283A>C
NM_001243254.1:c.3620A>C	NP_001230183.1:p.Asn1207Thr
NM_015213.3:c.3620A>C	NP_056028.2:p.Asn1207Thr
XM_005252832.1:c.3620A>C	XP_005252889.1:p.Asn1207Thr
XM_011519952.1:c.3620A>C	XP_011518254.1:p.Asn1207Thr
XM_011519953.1:c.1718A>C	XP_011518255.1:p.Asn573Thr
XR_242782.2:n.3802A>C
XR_930851.1:n.3802A>C
NM_001348749.1:c.3548A>C	NP_001335678.1:p.Asn1183Thr
NM_001348750.1:c.3332A>C	NP_001335679.1:p.Asn1111Thr
NR_145966.2:n.3794A>C
NM_015213.4:c.3620A>C MANE Select	NP_056028.2:p.Asn1207Thr
NM_001243254.2:c.3620A>C	NP_001230183.1:p.Asn1207Thr
NM_001348749.2:c.3548A>C	NP_001335678.1:p.Asn1183Thr
NM_001348750.2:c.3332A>C	NP_001335679.1:p.Asn1111Thr