Canonical Allele Identifier: CA1951464133
Gene: DENND5A HGNC NCBI

Linked Data

dbSNP Id: rs1847942827

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.9160488A>G , CM000673.2:g.9160488A>G GRCh38
NC_000011.9:g.9182035A>G , CM000673.1:g.9182035A>G GRCh37
NC_000011.8:g.9138611A>G NCBI36
NG_053019.1:g.109848T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000328194.8:c.2436+225T>C MANE Select ENSP00000328524.3:n.2436+225T>C
ENST00000530780.2:c.*2262+225T>C ENSP00000433925.1:n.*2262+225T>C
ENST00000679446.1:n.2357+225T>C
ENST00000679458.1:n.3837+225T>C
ENST00000679460.1:n.2225+225T>C
ENST00000679568.1:c.2436+225T>C ENSP00000505860.1:n.2436+225T>C
ENST00000679745.1:n.2225+225T>C
ENST00000679926.1:n.1252+225T>C
ENST00000679999.1:c.2436+225T>C ENSP00000505198.1:n.2436+225T>C
ENST00000680252.1:c.2225+225T>C
ENST00000680294.1:c.2436+225T>C ENSP00000506113.1:n.2436+225T>C
ENST00000680358.1:n.1735+225T>C
ENST00000680470.1:c.*302+225T>C ENSP00000505975.1:n.*302+225T>C
ENST00000680554.1:c.2148+225T>C ENSP00000505621.1:n.2148+225T>C
ENST00000680576.1:n.2225+225T>C
ENST00000680599.1:n.2353+225T>C
ENST00000680742.1:c.2436+225T>C ENSP00000505206.1:n.2436+225T>C
ENST00000680885.1:n.2357+225T>C
ENST00000681158.1:c.2225+225T>C
ENST00000681173.1:n.2226-189T>C
ENST00000681203.1:c.2364+225T>C ENSP00000506456.1:n.2364+225T>C
ENST00000681425.1:n.2357+225T>C
ENST00000328194.7:c.2436+225T>C ENSP00000328524.3:n.2436+225T>C
ENST00000526707.5:c.2364+225T>C ENSP00000436780.1:n.2364+225T>C
ENST00000527700.5:n.1998+225T>C
ENST00000530044.5:c.2436+225T>C ENSP00000435866.1:n.2436+225T>C
NM_001243254.1:c.2436+225T>C NP_001230183.1:n.2436+225T>C
NM_015213.3:c.2436+225T>C NP_056028.2:n.2436+225T>C
XM_005252832.1:c.2436+225T>C XP_005252889.1:n.2436+225T>C
XM_011519952.1:c.2436+225T>C XP_011518254.1:n.2436+225T>C
XM_011519953.1:c.534+225T>C XP_011518255.1:n.534+225T>C
XR_242782.2:n.2701+225T>C
XR_930851.1:n.2701+225T>C
XR_930852.1:n.2701+225T>C
XR_930853.1:n.2550+225T>C
NM_001348749.1:c.2364+225T>C NP_001335678.1:n.2364+225T>C
NM_001348750.1:c.2148+225T>C NP_001335679.1:n.2148+225T>C
NR_145966.2:n.2693+225T>C
NM_015213.4:c.2436+225T>C MANE Select NP_056028.2:n.2436+225T>C
NM_001243254.2:c.2436+225T>C NP_001230183.1:n.2436+225T>C
NM_001348749.2:c.2364+225T>C NP_001335678.1:n.2364+225T>C
NM_001348750.2:c.2148+225T>C NP_001335679.1:n.2148+225T>C