Canonical Allele Identifier: CA379599815

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9225683T>G (hg19) ; chr11:g.9204136T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9204136T>G , CM000673.2:g.9204136T>G	GRCh38
NC_000011.9:g.9225683T>G , CM000673.1:g.9225683T>G	GRCh37
NC_000011.8:g.9182259T>G	NCBI36
NG_053019.1:g.66200A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.473A>C MANE Select	ENSP00000328524.3:p.Asn158Thr
ENST00000530780.2:c.*299A>C	ENSP00000433925.1:n.*299A>C
ENST00000530867.2:n.262A>C
ENST00000532696.2:n.396A>C
ENST00000679446.1:n.394A>C
ENST00000679460.1:n.262A>C
ENST00000679568.1:c.473A>C	ENSP00000505860.1:p.Asn158Thr
ENST00000679745.1:n.262A>C
ENST00000679999.1:c.473A>C	ENSP00000505198.1:p.Asn158Thr
ENST00000680252.1:c.262A>C
ENST00000680294.1:c.473A>C	ENSP00000506113.1:p.Asn158Thr
ENST00000680470.1:c.473A>C	ENSP00000505975.1:p.Asn158Thr
ENST00000680554.1:c.185A>C	ENSP00000505621.1:p.Asn62Thr
ENST00000680576.1:n.262A>C
ENST00000680599.1:n.390A>C
ENST00000680742.1:c.473A>C	ENSP00000505206.1:p.Asn158Thr
ENST00000680885.1:n.394A>C
ENST00000681158.1:c.262A>C
ENST00000681173.1:n.262A>C
ENST00000681203.1:c.401A>C	ENSP00000506456.1:p.Asn134Thr
ENST00000681425.1:n.394A>C
ENST00000681915.1:n.262A>C
ENST00000328194.7:c.473A>C	ENSP00000328524.3:p.Asn158Thr
ENST00000526707.5:c.401A>C	ENSP00000436780.1:p.Asn134Thr
ENST00000530044.5:c.473A>C	ENSP00000435866.1:p.Asn158Thr
ENST00000530780.1:c.*299A>C	ENSP00000433925.1:n.*299A>C
ENST00000532696.1:n.228A>C
NM_001243254.1:c.473A>C	NP_001230183.1:p.Asn158Thr
NM_015213.3:c.473A>C	NP_056028.2:p.Asn158Thr
XM_005252832.1:c.473A>C	XP_005252889.1:p.Asn158Thr
XM_011519952.1:c.473A>C	XP_011518254.1:p.Asn158Thr
XR_242782.2:n.738A>C
XR_930851.1:n.738A>C
XR_930852.1:n.738A>C
XR_930853.1:n.738A>C
NM_001348749.1:c.401A>C	NP_001335678.1:p.Asn134Thr
NM_001348750.1:c.185A>C	NP_001335679.1:p.Asn62Thr
NR_145966.2:n.730A>C
NM_015213.4:c.473A>C MANE Select	NP_056028.2:p.Asn158Thr
NM_001243254.2:c.473A>C	NP_001230183.1:p.Asn158Thr
NM_001348749.2:c.401A>C	NP_001335678.1:p.Asn134Thr
NM_001348750.2:c.185A>C	NP_001335679.1:p.Asn62Thr