Canonical Allele Identifier: CA473254348

Gene: DENND5A

Linked Data

• MyVariant Identifiers: chr11:g.9225367A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9203820A>T , CM000673.2:g.9203820A>T	GRCh38
NC_000011.9:g.9225367A>T , CM000673.1:g.9225367A>T	GRCh37
NC_000011.8:g.9181943A>T	NCBI36
NG_053019.1:g.66516T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.789T>A MANE Select	ENSP00000328524.3:p.Ser263=
ENST00000530780.2:c.*615T>A	ENSP00000433925.1:n.*615T>A
ENST00000530867.2:n.578T>A
ENST00000532696.2:n.712T>A
ENST00000679446.1:n.710T>A
ENST00000679460.1:n.578T>A
ENST00000679568.1:c.789T>A	ENSP00000505860.1:p.Ser263=
ENST00000679745.1:n.578T>A
ENST00000679999.1:c.789T>A	ENSP00000505198.1:p.Ser263=
ENST00000680252.1:c.578T>A
ENST00000680294.1:c.789T>A	ENSP00000506113.1:p.Ser263=
ENST00000680470.1:c.789T>A	ENSP00000505975.1:p.Ser263=
ENST00000680554.1:c.501T>A	ENSP00000505621.1:p.Ser167=
ENST00000680576.1:n.578T>A
ENST00000680599.1:n.706T>A
ENST00000680742.1:c.789T>A	ENSP00000505206.1:p.Ser263=
ENST00000680885.1:n.710T>A
ENST00000681158.1:c.578T>A
ENST00000681173.1:n.578T>A
ENST00000681203.1:c.717T>A	ENSP00000506456.1:p.Ser239=
ENST00000681425.1:n.710T>A
ENST00000681915.1:n.578T>A
ENST00000328194.7:c.789T>A	ENSP00000328524.3:p.Ser263=
ENST00000526707.5:c.717T>A	ENSP00000436780.1:p.Ser239=
ENST00000530044.5:c.789T>A	ENSP00000435866.1:p.Ser263=
ENST00000532696.1:n.544T>A
NM_001243254.1:c.789T>A	NP_001230183.1:p.Ser263=
NM_015213.3:c.789T>A	NP_056028.2:p.Ser263=
XM_005252832.1:c.789T>A	XP_005252889.1:p.Ser263=
XM_011519952.1:c.789T>A	XP_011518254.1:p.Ser263=
XR_242782.2:n.1054T>A
XR_930851.1:n.1054T>A
XR_930852.1:n.1054T>A
XR_930853.1:n.1054T>A
NM_001348749.1:c.717T>A	NP_001335678.1:p.Ser239=
NM_001348750.1:c.501T>A	NP_001335679.1:p.Ser167=
NR_145966.2:n.1046T>A
NM_015213.4:c.789T>A MANE Select	NP_056028.2:p.Ser263=
NM_001243254.2:c.789T>A	NP_001230183.1:p.Ser263=
NM_001348749.2:c.717T>A	NP_001335678.1:p.Ser239=
NM_001348750.2:c.501T>A	NP_001335679.1:p.Ser167=