Canonical Allele Identifier: CA379598098

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163621C>G (hg19) ; chr11:g.9142074C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142074C>G , CM000673.2:g.9142074C>G	GRCh38
NC_000011.9:g.9163621C>G , CM000673.1:g.9163621C>G	GRCh37
NC_000011.8:g.9120197C>G	NCBI36
NG_053019.1:g.128262G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3546G>C MANE Select	ENSP00000328524.3:p.Lys1182Asn
ENST00000525784.6:n.1408G>C
ENST00000530780.2:c.*3372G>C	ENSP00000433925.1:n.*3372G>C
ENST00000531747.2:n.3217G>C
ENST00000679446.1:n.3467G>C
ENST00000679458.1:n.4947G>C
ENST00000679460.1:n.4608G>C
ENST00000679568.1:c.3546G>C	ENSP00000505860.1:p.Lys1182Asn
ENST00000679745.1:n.4051G>C
ENST00000679773.1:n.2707G>C
ENST00000679926.1:n.4848G>C
ENST00000679999.1:c.*603G>C	ENSP00000505198.1:n.*603G>C
ENST00000680252.1:c.3213G>C
ENST00000680294.1:c.3339G>C	ENSP00000506113.1:p.Lys1113Asn
ENST00000680358.1:n.2845G>C
ENST00000680470.1:c.*1327G>C	ENSP00000505975.1:n.*1327G>C
ENST00000680554.1:c.*79G>C	ENSP00000505621.1:n.*79G>C
ENST00000680576.1:n.5022G>C
ENST00000680599.1:n.3587G>C
ENST00000680742.1:c.*79G>C	ENSP00000505206.1:n.*79G>C
ENST00000680791.1:n.2430G>C
ENST00000680885.1:n.5248G>C
ENST00000681158.1:c.3130G>C
ENST00000681203.1:c.3474G>C	ENSP00000506456.1:p.Lys1158Asn
ENST00000681371.1:n.3418G>C
ENST00000681425.1:n.4024G>C
ENST00000681639.1:n.1825G>C
ENST00000328194.7:c.3546G>C	ENSP00000328524.3:p.Lys1182Asn
ENST00000525784.5:c.482G>C
ENST00000527700.5:n.3108G>C
ENST00000528725.5:c.242G>C
ENST00000529977.5:n.1447G>C
ENST00000530044.5:c.3546G>C	ENSP00000435866.1:p.Lys1182Asn
ENST00000531747.1:c.782G>C
ENST00000533737.5:c.209G>C
NM_001243254.1:c.3546G>C	NP_001230183.1:p.Lys1182Asn
NM_015213.3:c.3546G>C	NP_056028.2:p.Lys1182Asn
XM_005252832.1:c.3546G>C	XP_005252889.1:p.Lys1182Asn
XM_011519952.1:c.3546G>C	XP_011518254.1:p.Lys1182Asn
XM_011519953.1:c.1644G>C	XP_011518255.1:p.Lys548Asn
XR_242782.2:n.3728G>C
XR_930851.1:n.3728G>C
NM_001348749.1:c.3474G>C	NP_001335678.1:p.Lys1158Asn
NM_001348750.1:c.3258G>C	NP_001335679.1:p.Lys1086Asn
NR_145966.2:n.3720G>C
NM_015213.4:c.3546G>C MANE Select	NP_056028.2:p.Lys1182Asn
NM_001243254.2:c.3546G>C	NP_001230183.1:p.Lys1182Asn
NM_001348749.2:c.3474G>C	NP_001335678.1:p.Lys1158Asn
NM_001348750.2:c.3258G>C	NP_001335679.1:p.Lys1086Asn