Canonical Allele Identifier: CA473040181

Gene: DENND5A

Linked Data

• gnomAD v4: 11-9141942-G-C
• MyVariant Identifiers: chr11:g.9163489G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9141942G>C , CM000673.2:g.9141942G>C	GRCh38
NC_000011.9:g.9163489G>C , CM000673.1:g.9163489G>C	GRCh37
NC_000011.8:g.9120065G>C	NCBI36
NG_053019.1:g.128394C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328194.8:c.3678C>G MANE Select	ENSP00000328524.3:p.Ala1226=
ENST00000525784.6:n.1540C>G
ENST00000530780.2:c.*3504C>G	ENSP00000433925.1:n.*3504C>G
ENST00000531747.2:n.3349C>G
ENST00000679446.1:n.3599C>G
ENST00000679458.1:n.5079C>G
ENST00000679460.1:n.4740C>G
ENST00000679568.1:c.3678C>G	ENSP00000505860.1:p.Ala1226=
ENST00000679745.1:n.4183C>G
ENST00000679773.1:n.2839C>G
ENST00000679926.1:n.4980C>G
ENST00000679999.1:c.*735C>G	ENSP00000505198.1:n.*735C>G
ENST00000680252.1:c.3345C>G
ENST00000680294.1:c.3471C>G	ENSP00000506113.1:p.Ala1157=
ENST00000680358.1:n.2977C>G
ENST00000680470.1:c.*1459C>G	ENSP00000505975.1:n.*1459C>G
ENST00000680554.1:c.*211C>G	ENSP00000505621.1:n.*211C>G
ENST00000680576.1:n.5154C>G
ENST00000680599.1:n.3719C>G
ENST00000680742.1:c.*179+32C>G	ENSP00000505206.1:n.*179+32C>G
ENST00000680791.1:n.2562C>G
ENST00000680885.1:n.5380C>G
ENST00000681158.1:c.3262C>G
ENST00000681203.1:c.3606C>G	ENSP00000506456.1:p.Ala1202=
ENST00000681371.1:n.3550C>G
ENST00000681425.1:n.4156C>G
ENST00000681639.1:n.1957C>G
ENST00000328194.7:c.3678C>G	ENSP00000328524.3:p.Ala1226=
ENST00000525784.5:c.614C>G
ENST00000527700.5:n.3240C>G
ENST00000528725.5:c.374C>G
ENST00000529977.5:n.1579C>G
ENST00000530044.5:c.3646+32C>G	ENSP00000435866.1:n.3646+32C>G
ENST00000531747.1:c.914C>G
ENST00000533737.5:c.341C>G
NM_001243254.1:c.3646+32C>G	NP_001230183.1:n.3646+32C>G
NM_015213.3:c.3678C>G	NP_056028.2:p.Ala1226=
XM_005252832.1:c.3678C>G	XP_005252889.1:p.Ala1226=
XM_011519952.1:c.3646+32C>G	XP_011518254.1:n.3646+32C>G
XM_011519953.1:c.1776C>G	XP_011518255.1:p.Ala592=
XR_242782.2:n.3860C>G
XR_930851.1:n.3828+32C>G
NM_001348749.1:c.3606C>G	NP_001335678.1:p.Ala1202=
NM_001348750.1:c.3390C>G	NP_001335679.1:p.Ala1130=
NR_145966.2:n.3852C>G
NM_015213.4:c.3678C>G MANE Select	NP_056028.2:p.Ala1226=
NM_001243254.2:c.3646+32C>G	NP_001230183.1:n.3646+32C>G
NM_001348749.2:c.3606C>G	NP_001335678.1:p.Ala1202=
NM_001348750.2:c.3390C>G	NP_001335679.1:p.Ala1130=