Canonical Allele Identifier: CA1951491988
Gene: DENND5A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9204004_9204006delinsTAG , CM000673.2:g.9204004_9204006delinsTAG GRCh38
NC_000011.9:g.9225551_9225553delinsTAG , CM000673.1:g.9225551_9225553delinsTAG GRCh37
NC_000011.8:g.9182127_9182129delinsTAG NCBI36
NG_053019.1:g.66330_66332delinsCTA

Transcript Alleles

HGVS Amino-acid change
ENST00000328194.8:c.603_605delinsCTA MANE Select ENSP00000328524.3:p.Leu201=
ENST00000530780.2:c.*429_*431delinsCTA ENSP00000433925.1:n.*429_*431delinsCTA
ENST00000530867.2:n.392_394delinsCTA
ENST00000532696.2:n.526_528delinsCTA
ENST00000679446.1:n.524_526delinsCTA
ENST00000679460.1:n.392_394delinsCTA
ENST00000679568.1:c.603_605delinsCTA ENSP00000505860.1:p.Leu201=
ENST00000679745.1:n.392_394delinsCTA
ENST00000679999.1:c.603_605delinsCTA ENSP00000505198.1:p.Leu201=
ENST00000680252.1:c.392_394delinsCTA
ENST00000680294.1:c.603_605delinsCTA ENSP00000506113.1:p.Leu201=
ENST00000680470.1:c.603_605delinsCTA ENSP00000505975.1:p.Leu201=
ENST00000680554.1:c.315_317delinsCTA ENSP00000505621.1:p.Leu105=
ENST00000680576.1:n.392_394delinsCTA
ENST00000680599.1:n.520_522delinsCTA
ENST00000680742.1:c.603_605delinsCTA ENSP00000505206.1:p.Leu201=
ENST00000680885.1:n.524_526delinsCTA
ENST00000681158.1:c.392_394delinsCTA
ENST00000681173.1:n.392_394delinsCTA
ENST00000681203.1:c.531_533delinsCTA ENSP00000506456.1:p.Leu177=
ENST00000681425.1:n.524_526delinsCTA
ENST00000681915.1:n.392_394delinsCTA
ENST00000328194.7:c.603_605delinsCTA ENSP00000328524.3:p.Leu201=
ENST00000526707.5:c.531_533delinsCTA ENSP00000436780.1:p.Leu177=
ENST00000530044.5:c.603_605delinsCTA ENSP00000435866.1:p.Leu201=
ENST00000532696.1:n.358_360delinsCTA
NM_001243254.1:c.603_605delinsCTA NP_001230183.1:p.Leu201=
NM_015213.3:c.603_605delinsCTA NP_056028.2:p.Leu201=
XM_005252832.1:c.603_605delinsCTA XP_005252889.1:p.Leu201=
XM_011519952.1:c.603_605delinsCTA XP_011518254.1:p.Leu201=
XR_242782.2:n.868_870delinsCTA
XR_930851.1:n.868_870delinsCTA
XR_930852.1:n.868_870delinsCTA
XR_930853.1:n.868_870delinsCTA
NM_001348749.1:c.531_533delinsCTA NP_001335678.1:p.Leu177=
NM_001348750.1:c.315_317delinsCTA NP_001335679.1:p.Leu105=
NR_145966.2:n.860_862delinsCTA
NM_015213.4:c.603_605delinsCTA MANE Select NP_056028.2:p.Leu201=
NM_001243254.2:c.603_605delinsCTA NP_001230183.1:p.Leu201=
NM_001348749.2:c.531_533delinsCTA NP_001335678.1:p.Leu177=
NM_001348750.2:c.315_317delinsCTA NP_001335679.1:p.Leu105=