Canonical Allele Identifier: CA473040222

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9163558A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9142011A>C , CM000673.2:g.9142011A>C	GRCh38
NC_000011.9:g.9163558A>C , CM000673.1:g.9163558A>C	GRCh37
NC_000011.8:g.9120134A>C	NCBI36
NG_053019.1:g.128325T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3609T>G MANE Select	ENSP00000328524.3:p.Thr1203=
ENST00000525784.6:n.1471T>G
ENST00000530780.2:c.*3435T>G	ENSP00000433925.1:n.*3435T>G
ENST00000531747.2:n.3280T>G
ENST00000679446.1:n.3530T>G
ENST00000679458.1:n.5010T>G
ENST00000679460.1:n.4671T>G
ENST00000679568.1:c.3609T>G	ENSP00000505860.1:p.Thr1203=
ENST00000679745.1:n.4114T>G
ENST00000679773.1:n.2770T>G
ENST00000679926.1:n.4911T>G
ENST00000679999.1:c.*666T>G	ENSP00000505198.1:n.*666T>G
ENST00000680252.1:c.3276T>G
ENST00000680294.1:c.3402T>G	ENSP00000506113.1:p.Thr1134=
ENST00000680358.1:n.2908T>G
ENST00000680470.1:c.*1390T>G	ENSP00000505975.1:n.*1390T>G
ENST00000680554.1:c.*142T>G	ENSP00000505621.1:n.*142T>G
ENST00000680576.1:n.5085T>G
ENST00000680599.1:n.3650T>G
ENST00000680742.1:c.*142T>G	ENSP00000505206.1:n.*142T>G
ENST00000680791.1:n.2493T>G
ENST00000680885.1:n.5311T>G
ENST00000681158.1:c.3193T>G
ENST00000681203.1:c.3537T>G	ENSP00000506456.1:p.Thr1179=
ENST00000681371.1:n.3481T>G
ENST00000681425.1:n.4087T>G
ENST00000681639.1:n.1888T>G
ENST00000328194.7:c.3609T>G	ENSP00000328524.3:p.Thr1203=
ENST00000525784.5:c.545T>G
ENST00000527700.5:n.3171T>G
ENST00000528725.5:c.305T>G
ENST00000529977.5:n.1510T>G
ENST00000530044.5:c.3609T>G	ENSP00000435866.1:p.Thr1203=
ENST00000531747.1:c.845T>G
ENST00000533737.5:c.272T>G
NM_001243254.1:c.3609T>G	NP_001230183.1:p.Thr1203=
NM_015213.3:c.3609T>G	NP_056028.2:p.Thr1203=
XM_005252832.1:c.3609T>G	XP_005252889.1:p.Thr1203=
XM_011519952.1:c.3609T>G	XP_011518254.1:p.Thr1203=
XM_011519953.1:c.1707T>G	XP_011518255.1:p.Thr569=
XR_242782.2:n.3791T>G
XR_930851.1:n.3791T>G
NM_001348749.1:c.3537T>G	NP_001335678.1:p.Thr1179=
NM_001348750.1:c.3321T>G	NP_001335679.1:p.Thr1107=
NR_145966.2:n.3783T>G
NM_015213.4:c.3609T>G MANE Select	NP_056028.2:p.Thr1203=
NM_001243254.2:c.3609T>G	NP_001230183.1:p.Thr1203=
NM_001348749.2:c.3537T>G	NP_001335678.1:p.Thr1179=
NM_001348750.2:c.3321T>G	NP_001335679.1:p.Thr1107=