Canonical Allele Identifier: CA379598264

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163651T>G (hg19) ; chr11:g.9142104T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142104T>G , CM000673.2:g.9142104T>G	GRCh38
NC_000011.9:g.9163651T>G , CM000673.1:g.9163651T>G	GRCh37
NC_000011.8:g.9120227T>G	NCBI36
NG_053019.1:g.128232A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3516A>C MANE Select	ENSP00000328524.3:p.Lys1172Asn
ENST00000525784.6:n.1378A>C
ENST00000530780.2:c.*3342A>C	ENSP00000433925.1:n.*3342A>C
ENST00000531747.2:n.3187A>C
ENST00000679446.1:n.3437A>C
ENST00000679458.1:n.4917A>C
ENST00000679460.1:n.4578A>C
ENST00000679568.1:c.3516A>C	ENSP00000505860.1:p.Lys1172Asn
ENST00000679745.1:n.4021A>C
ENST00000679773.1:n.2677A>C
ENST00000679926.1:n.4818A>C
ENST00000679999.1:c.*573A>C	ENSP00000505198.1:n.*573A>C
ENST00000680252.1:c.3183A>C
ENST00000680294.1:c.3309A>C	ENSP00000506113.1:p.Lys1103Asn
ENST00000680358.1:n.2815A>C
ENST00000680470.1:c.*1297A>C	ENSP00000505975.1:n.*1297A>C
ENST00000680554.1:c.*49A>C	ENSP00000505621.1:n.*49A>C
ENST00000680576.1:n.4992A>C
ENST00000680599.1:n.3557A>C
ENST00000680742.1:c.*49A>C	ENSP00000505206.1:n.*49A>C
ENST00000680791.1:n.2400A>C
ENST00000680885.1:n.5218A>C
ENST00000681158.1:c.3100A>C
ENST00000681203.1:c.3444A>C	ENSP00000506456.1:p.Lys1148Asn
ENST00000681371.1:n.3388A>C
ENST00000681425.1:n.3994A>C
ENST00000681639.1:n.1795A>C
ENST00000328194.7:c.3516A>C	ENSP00000328524.3:p.Lys1172Asn
ENST00000525784.5:c.452A>C
ENST00000527700.5:n.3078A>C
ENST00000528725.5:c.212A>C
ENST00000529977.5:n.1417A>C
ENST00000530044.5:c.3516A>C	ENSP00000435866.1:p.Lys1172Asn
ENST00000531747.1:c.752A>C
ENST00000533737.5:c.179A>C
NM_001243254.1:c.3516A>C	NP_001230183.1:p.Lys1172Asn
NM_015213.3:c.3516A>C	NP_056028.2:p.Lys1172Asn
XM_005252832.1:c.3516A>C	XP_005252889.1:p.Lys1172Asn
XM_011519952.1:c.3516A>C	XP_011518254.1:p.Lys1172Asn
XM_011519953.1:c.1614A>C	XP_011518255.1:p.Lys538Asn
XR_242782.2:n.3698A>C
XR_930851.1:n.3698A>C
NM_001348749.1:c.3444A>C	NP_001335678.1:p.Lys1148Asn
NM_001348750.1:c.3228A>C	NP_001335679.1:p.Lys1076Asn
NR_145966.2:n.3690A>C
NM_015213.4:c.3516A>C MANE Select	NP_056028.2:p.Lys1172Asn
NM_001243254.2:c.3516A>C	NP_001230183.1:p.Lys1172Asn
NM_001348749.2:c.3444A>C	NP_001335678.1:p.Lys1148Asn
NM_001348750.2:c.3228A>C	NP_001335679.1:p.Lys1076Asn