Canonical Allele Identifier: CA379598635
Gene: DENND5A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9203961C>T , CM000673.2:g.9203961C>T GRCh38
NC_000011.9:g.9225508C>T , CM000673.1:g.9225508C>T GRCh37
NC_000011.8:g.9182084C>T NCBI36
NG_053019.1:g.66375G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.648G>A MANE Select ENSP00000328524.3:p.Met216Ile
ENST00000530780.2:c.*474G>A ENSP00000433925.1:n.*474G>A
ENST00000530867.2:n.437G>A
ENST00000532696.2:n.571G>A
ENST00000679446.1:n.569G>A
ENST00000679460.1:n.437G>A
ENST00000679568.1:c.648G>A ENSP00000505860.1:p.Met216Ile
ENST00000679745.1:n.437G>A
ENST00000679999.1:c.648G>A ENSP00000505198.1:p.Met216Ile
ENST00000680252.1:c.437G>A
ENST00000680294.1:c.648G>A ENSP00000506113.1:p.Met216Ile
ENST00000680470.1:c.648G>A ENSP00000505975.1:p.Met216Ile
ENST00000680554.1:c.360G>A ENSP00000505621.1:p.Met120Ile
ENST00000680576.1:n.437G>A
ENST00000680599.1:n.565G>A
ENST00000680742.1:c.648G>A ENSP00000505206.1:p.Met216Ile
ENST00000680885.1:n.569G>A
ENST00000681158.1:c.437G>A
ENST00000681173.1:n.437G>A
ENST00000681203.1:c.576G>A ENSP00000506456.1:p.Met192Ile
ENST00000681425.1:n.569G>A
ENST00000681915.1:n.437G>A
ENST00000328194.7:c.648G>A ENSP00000328524.3:p.Met216Ile
ENST00000526707.5:c.576G>A ENSP00000436780.1:p.Met192Ile
ENST00000530044.5:c.648G>A ENSP00000435866.1:p.Met216Ile
ENST00000532696.1:n.403G>A
NM_001243254.1:c.648G>A NP_001230183.1:p.Met216Ile
NM_015213.3:c.648G>A NP_056028.2:p.Met216Ile
XM_005252832.1:c.648G>A XP_005252889.1:p.Met216Ile
XM_011519952.1:c.648G>A XP_011518254.1:p.Met216Ile
XR_242782.2:n.913G>A
XR_930851.1:n.913G>A
XR_930852.1:n.913G>A
XR_930853.1:n.913G>A
NM_001348749.1:c.576G>A NP_001335678.1:p.Met192Ile
NM_001348750.1:c.360G>A NP_001335679.1:p.Met120Ile
NR_145966.2:n.905G>A
NM_015213.4:c.648G>A MANE Select NP_056028.2:p.Met216Ile
NM_001243254.2:c.648G>A NP_001230183.1:p.Met216Ile
NM_001348749.2:c.576G>A NP_001335678.1:p.Met192Ile
NM_001348750.2:c.360G>A NP_001335679.1:p.Met120Ile