Canonical Allele Identifier: CA859802585

Gene: DENND1A

Linked Data

• dbSNP Id: rs1232080569
• MyVariant Identifiers: chr9:g.126525133G>C (hg19) ; chr9:g.123762854G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.123762854G>C , CM000671.2:g.123762854G>C	GRCh38
NC_000009.11:g.126525133G>C , CM000671.1:g.126525133G>C	GRCh37
NC_000009.10:g.125564954G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394215.7:c.183-5032C>G MANE Select	ENSP00000377763.4:n.183-5032C>G
ENST00000373618.1:c.87-5032C>G	ENSP00000362720.1:n.87-5032C>G
ENST00000373620.7:c.183-5032C>G	ENSP00000362722.3:n.183-5032C>G
ENST00000373624.6:c.183-5032C>G	ENSP00000362727.2:n.183-5032C>G
ENST00000473039.5:n.350-5032C>G
NM_020946.1:c.183-5032C>G	NP_065997.1:n.183-5032C>G
NM_024820.2:c.183-5032C>G	NP_079096.2:n.183-5032C>G
XM_005252109.2:c.183-5032C>G	XP_005252166.1:n.183-5032C>G
XM_005252111.3:c.228-5032C>G	XP_005252168.1:n.228-5032C>G
XM_005252113.3:c.228-5032C>G	XP_005252170.1:n.228-5032C>G
XM_006717195.2:c.228-5032C>G	XP_006717258.1:n.228-5032C>G
XM_011518882.1:c.228-5032C>G	XP_011517184.1:n.228-5032C>G
XM_011518883.1:c.228-5032C>G	XP_011517185.1:n.228-5032C>G
XM_011518884.1:c.141-5032C>G	XP_011517186.1:n.141-5032C>G
XM_011518885.1:c.120-5032C>G	XP_011517187.1:n.120-5032C>G
XM_011518886.1:c.228-5032C>G	XP_011517188.1:n.228-5032C>G
XM_011518887.1:c.228-5032C>G	XP_011517189.1:n.228-5032C>G
XR_929829.1:n.1216-5032C>G
XR_929830.1:n.1213-5032C>G
NM_001352964.1:c.183-5032C>G	NP_001339893.1:n.183-5032C>G
NM_001352965.1:c.87-5032C>G	NP_001339894.1:n.87-5032C>G
NM_001352966.1:c.93-5032C>G	NP_001339895.1:n.93-5032C>G
NM_001352967.1:c.87-5032C>G	NP_001339896.1:n.87-5032C>G
NM_001352968.1:c.87-5032C>G	NP_001339897.1:n.87-5032C>G
NR_148208.1:n.416-5032C>G
XM_005252111.4:c.228-5032C>G	XP_005252168.1:n.228-5032C>G
XM_005252113.5:c.228-5032C>G	XP_005252170.1:n.228-5032C>G
XM_006717195.4:c.228-5032C>G	XP_006717258.1:n.228-5032C>G
XM_011518882.3:c.228-5032C>G	XP_011517184.1:n.228-5032C>G
XM_011518883.3:c.228-5032C>G	XP_011517185.1:n.228-5032C>G
XM_011518885.3:c.120-5032C>G	XP_011517187.1:n.120-5032C>G
XM_011518886.3:c.228-5032C>G	XP_011517188.1:n.228-5032C>G
XM_011518887.3:c.228-5032C>G	XP_011517189.1:n.228-5032C>G
XM_017014948.2:c.183-5032C>G	XP_016870437.1:n.183-5032C>G
XM_017014949.2:c.228-5032C>G	XP_016870438.1:n.228-5032C>G
XM_017014950.2:c.228-5032C>G	XP_016870439.1:n.228-5032C>G
XM_017014951.2:c.87-5032C>G	XP_016870440.1:n.87-5032C>G
XM_017014952.2:c.-549-5032C>G	XP_016870441.1:n.-549-5032C>G
XM_024447621.1:c.87-5032C>G	XP_024303389.1:n.87-5032C>G
XM_024447622.1:c.93-5032C>G	XP_024303390.1:n.93-5032C>G
XM_024447624.1:c.228-5032C>G	XP_024303392.1:n.228-5032C>G
XR_929829.2:n.1225-5032C>G
XR_929830.3:n.1222-5032C>G
NM_001352966.2:c.93-5032C>G	NP_001339895.1:n.93-5032C>G
NM_001352967.2:c.87-5032C>G	NP_001339896.1:n.87-5032C>G
NM_001352968.2:c.87-5032C>G	NP_001339897.1:n.87-5032C>G
NM_024820.3:c.183-5032C>G	NP_079096.2:n.183-5032C>G
NR_148208.2:n.404-5032C>G
NM_001352964.2:c.183-5032C>G MANE Select	NP_001339893.1:n.183-5032C>G
NM_001352965.2:c.87-5032C>G	NP_001339894.1:n.87-5032C>G
NM_001393654.1:c.183-5032C>G	NP_001380583.1:n.183-5032C>G
NM_020946.2:c.183-5032C>G	NP_065997.1:n.183-5032C>G
NM_001400446.1:c.93-5032C>G	NP_001387375.1:n.93-5032C>G
NM_001400449.1:c.87-5032C>G	NP_001387378.1:n.87-5032C>G