Canonical Allele Identifier: CA379599029
Gene: DENND5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9204008G>A , CM000673.2:g.9204008G>A GRCh38
NC_000011.9:g.9225555G>A , CM000673.1:g.9225555G>A GRCh37
NC_000011.8:g.9182131G>A NCBI36
NG_053019.1:g.66328C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.601C>T MANE Select ENSP00000328524.3:p.Leu201Phe
ENST00000530780.2:c.*427C>T ENSP00000433925.1:n.*427C>T
ENST00000530867.2:n.390C>T
ENST00000532696.2:n.524C>T
ENST00000679446.1:n.522C>T
ENST00000679460.1:n.390C>T
ENST00000679568.1:c.601C>T ENSP00000505860.1:p.Leu201Phe
ENST00000679745.1:n.390C>T
ENST00000679999.1:c.601C>T ENSP00000505198.1:p.Leu201Phe
ENST00000680252.1:c.390C>T
ENST00000680294.1:c.601C>T ENSP00000506113.1:p.Leu201Phe
ENST00000680470.1:c.601C>T ENSP00000505975.1:p.Leu201Phe
ENST00000680554.1:c.313C>T ENSP00000505621.1:p.Leu105Phe
ENST00000680576.1:n.390C>T
ENST00000680599.1:n.518C>T
ENST00000680742.1:c.601C>T ENSP00000505206.1:p.Leu201Phe
ENST00000680885.1:n.522C>T
ENST00000681158.1:c.390C>T
ENST00000681173.1:n.390C>T
ENST00000681203.1:c.529C>T ENSP00000506456.1:p.Leu177Phe
ENST00000681425.1:n.522C>T
ENST00000681915.1:n.390C>T
ENST00000328194.7:c.601C>T ENSP00000328524.3:p.Leu201Phe
ENST00000526707.5:c.529C>T ENSP00000436780.1:p.Leu177Phe
ENST00000530044.5:c.601C>T ENSP00000435866.1:p.Leu201Phe
ENST00000532696.1:n.356C>T
NM_001243254.1:c.601C>T NP_001230183.1:p.Leu201Phe
NM_015213.3:c.601C>T NP_056028.2:p.Leu201Phe
XM_005252832.1:c.601C>T XP_005252889.1:p.Leu201Phe
XM_011519952.1:c.601C>T XP_011518254.1:p.Leu201Phe
XR_242782.2:n.866C>T
XR_930851.1:n.866C>T
XR_930852.1:n.866C>T
XR_930853.1:n.866C>T
NM_001348749.1:c.529C>T NP_001335678.1:p.Leu177Phe
NM_001348750.1:c.313C>T NP_001335679.1:p.Leu105Phe
NR_145966.2:n.858C>T
NM_015213.4:c.601C>T MANE Select NP_056028.2:p.Leu201Phe
NM_001243254.2:c.601C>T NP_001230183.1:p.Leu201Phe
NM_001348749.2:c.529C>T NP_001335678.1:p.Leu177Phe
NM_001348750.2:c.313C>T NP_001335679.1:p.Leu105Phe