Canonical Allele Identifier: CA1951464241

Gene: DENND5A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9160635_9160636delinsCA , CM000673.2:g.9160635_9160636delinsCA	GRCh38
NC_000011.9:g.9182182_9182183delinsCA , CM000673.1:g.9182182_9182183delinsCA	GRCh37
NC_000011.8:g.9138758_9138759delinsCA	NCBI36
NG_053019.1:g.109700_109701delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.2436+77_2436+78delinsTG MANE Select	ENSP00000328524.3:n.2436+77_2436+78delinsTG
ENST00000530780.2:c.*2262+77_*2262+78delinsTG	ENSP00000433925.1:n.*2262+77_*2262+78delinsTG
ENST00000679446.1:n.2357+77_2357+78delinsTG
ENST00000679458.1:n.3837+77_3837+78delinsTG
ENST00000679460.1:n.2225+77_2225+78delinsTG
ENST00000679568.1:c.2436+77_2436+78delinsTG	ENSP00000505860.1:n.2436+77_2436+78delinsTG
ENST00000679745.1:n.2225+77_2225+78delinsTG
ENST00000679926.1:n.1252+77_1252+78delinsTG
ENST00000679999.1:c.2436+77_2436+78delinsTG	ENSP00000505198.1:n.2436+77_2436+78delinsTG
ENST00000680252.1:c.2225+77_2225+78delinsTG
ENST00000680294.1:c.2436+77_2436+78delinsTG	ENSP00000506113.1:n.2436+77_2436+78delinsTG
ENST00000680358.1:n.1735+77_1735+78delinsTG
ENST00000680470.1:c.*302+77_*302+78delinsTG	ENSP00000505975.1:n.*302+77_*302+78delinsTG
ENST00000680554.1:c.2148+77_2148+78delinsTG	ENSP00000505621.1:n.2148+77_2148+78delinsTG
ENST00000680576.1:n.2225+77_2225+78delinsTG
ENST00000680599.1:n.2353+77_2353+78delinsTG
ENST00000680742.1:c.2436+77_2436+78delinsTG	ENSP00000505206.1:n.2436+77_2436+78delinsTG
ENST00000680885.1:n.2357+77_2357+78delinsTG
ENST00000681158.1:c.2225+77_2225+78delinsTG
ENST00000681173.1:n.2225+77_2225+78delinsTG
ENST00000681203.1:c.2364+77_2364+78delinsTG	ENSP00000506456.1:n.2364+77_2364+78delinsTG
ENST00000681425.1:n.2357+77_2357+78delinsTG
ENST00000328194.7:c.2436+77_2436+78delinsTG	ENSP00000328524.3:n.2436+77_2436+78delinsTG
ENST00000526707.5:c.2364+77_2364+78delinsTG	ENSP00000436780.1:n.2364+77_2364+78delinsTG
ENST00000527700.5:n.1998+77_1998+78delinsTG
ENST00000530044.5:c.2436+77_2436+78delinsTG	ENSP00000435866.1:n.2436+77_2436+78delinsTG
NM_001243254.1:c.2436+77_2436+78delinsTG	NP_001230183.1:n.2436+77_2436+78delinsTG
NM_015213.3:c.2436+77_2436+78delinsTG	NP_056028.2:n.2436+77_2436+78delinsTG
XM_005252832.1:c.2436+77_2436+78delinsTG	XP_005252889.1:n.2436+77_2436+78delinsTG
XM_011519952.1:c.2436+77_2436+78delinsTG	XP_011518254.1:n.2436+77_2436+78delinsTG
XM_011519953.1:c.534+77_534+78delinsTG	XP_011518255.1:n.534+77_534+78delinsTG
XR_242782.2:n.2701+77_2701+78delinsTG
XR_930851.1:n.2701+77_2701+78delinsTG
XR_930852.1:n.2701+77_2701+78delinsTG
XR_930853.1:n.2550+77_2550+78delinsTG
NM_001348749.1:c.2364+77_2364+78delinsTG	NP_001335678.1:n.2364+77_2364+78delinsTG
NM_001348750.1:c.2148+77_2148+78delinsTG	NP_001335679.1:n.2148+77_2148+78delinsTG
NR_145966.2:n.2693+77_2693+78delinsTG
NM_015213.4:c.2436+77_2436+78delinsTG MANE Select	NP_056028.2:n.2436+77_2436+78delinsTG
NM_001243254.2:c.2436+77_2436+78delinsTG	NP_001230183.1:n.2436+77_2436+78delinsTG
NM_001348749.2:c.2364+77_2364+78delinsTG	NP_001335678.1:n.2364+77_2364+78delinsTG
NM_001348750.2:c.2148+77_2148+78delinsTG	NP_001335679.1:n.2148+77_2148+78delinsTG