Canonical Allele Identifier: CA199485357
Gene: DENND1A HGNC NCBI

Linked Data

dbSNP Id: rs7037102
gnomAD v2: 9-126317639-G-A
gnomAD v3: 9-123555360-G-A
gnomAD v4: 9-123555360-G-A
MyVariant Identifiers: chr9:g.126317639G>A (hg19) chr9:g.123555360G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.123555360G>A , CM000671.2:g.123555360G>A GRCh38
NC_000009.11:g.126317639G>A , CM000671.1:g.126317639G>A GRCh37
NC_000009.10:g.125357460G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000699491.1:c.691+2210C>T
ENST00000394215.7:c.993+2210C>T MANE Select ENSP00000377763.4:n.993+2210C>T
ENST00000373618.1:c.897+2210C>T ENSP00000362720.1:n.897+2210C>T
ENST00000373620.7:c.993+2210C>T ENSP00000362722.3:n.993+2210C>T
ENST00000373624.6:c.993+2210C>T ENSP00000362727.2:n.993+2210C>T
ENST00000394215.6:c.693+2210C>T ENSP00000377763.3:n.693+2210C>T
ENST00000394219.7:c.693+2210C>T ENSP00000377766.4:n.693+2210C>T
ENST00000473039.5:n.1090+2210C>T
ENST00000491650.5:n.246+2210C>T
ENST00000497135.5:n.175+2210C>T
NM_020946.1:c.993+2210C>T NP_065997.1:n.993+2210C>T
NM_024820.2:c.993+2210C>T NP_079096.2:n.993+2210C>T
XM_005252109.2:c.993+2210C>T XP_005252166.1:n.993+2210C>T
XM_005252111.3:c.1038+2210C>T XP_005252168.1:n.1038+2210C>T
XM_005252113.3:c.1038+2210C>T XP_005252170.1:n.1038+2210C>T
XM_006717195.2:c.1038+2210C>T XP_006717258.1:n.1038+2210C>T
XM_011518882.1:c.1038+2210C>T XP_011517184.1:n.1038+2210C>T
XM_011518883.1:c.1038+2210C>T XP_011517185.1:n.1038+2210C>T
XM_011518884.1:c.951+2210C>T XP_011517186.1:n.951+2210C>T
XM_011518885.1:c.930+2210C>T XP_011517187.1:n.930+2210C>T
XM_011518886.1:c.1038+2210C>T XP_011517188.1:n.1038+2210C>T
XM_011518887.1:c.1038+2210C>T XP_011517189.1:n.1038+2210C>T
XR_929829.1:n.2026+2210C>T
XR_929830.1:n.2023+2210C>T
NM_001352964.1:c.993+2210C>T NP_001339893.1:n.993+2210C>T
NM_001352965.1:c.897+2210C>T NP_001339894.1:n.897+2210C>T
NM_001352966.1:c.903+2210C>T NP_001339895.1:n.903+2210C>T
NM_001352967.1:c.897+2210C>T NP_001339896.1:n.897+2210C>T
NM_001352968.1:c.897+2210C>T NP_001339897.1:n.897+2210C>T
NR_148208.1:n.1230+2206C>T
XM_005252111.4:c.1038+2210C>T XP_005252168.1:n.1038+2210C>T
XM_005252113.5:c.1038+2210C>T XP_005252170.1:n.1038+2210C>T
XM_006717195.4:c.1038+2210C>T XP_006717258.1:n.1038+2210C>T
XM_011518882.3:c.1038+2210C>T XP_011517184.1:n.1038+2210C>T
XM_011518883.3:c.1038+2210C>T XP_011517185.1:n.1038+2210C>T
XM_011518885.3:c.930+2210C>T XP_011517187.1:n.930+2210C>T
XM_011518886.3:c.1038+2210C>T XP_011517188.1:n.1038+2210C>T
XM_011518887.3:c.1038+2210C>T XP_011517189.1:n.1038+2210C>T
XM_017014948.2:c.993+2210C>T XP_016870437.1:n.993+2210C>T
XM_017014949.2:c.912+27809C>T XP_016870438.1:n.912+27809C>T
XM_017014950.2:c.912+27809C>T XP_016870439.1:n.912+27809C>T
XM_017014951.2:c.897+2210C>T XP_016870440.1:n.897+2210C>T
XM_017014952.2:c.216+2210C>T XP_016870441.1:n.216+2210C>T
XM_024447621.1:c.897+2210C>T XP_024303389.1:n.897+2210C>T
XM_024447622.1:c.903+2210C>T XP_024303390.1:n.903+2210C>T
XM_024447623.1:c.405+2210C>T XP_024303391.1:n.405+2210C>T
XM_024447624.1:c.1038+2210C>T XP_024303392.1:n.1038+2210C>T
XR_929829.2:n.2035+2210C>T
XR_929830.3:n.2032+2210C>T
NM_001352966.2:c.903+2210C>T NP_001339895.1:n.903+2210C>T
NM_001352967.2:c.897+2210C>T NP_001339896.1:n.897+2210C>T
NM_001352968.2:c.897+2210C>T NP_001339897.1:n.897+2210C>T
NM_024820.3:c.993+2210C>T NP_079096.2:n.993+2210C>T
NR_148208.2:n.1218+2206C>T
NM_001352964.2:c.993+2210C>T MANE Select NP_001339893.1:n.993+2210C>T
NM_001352965.2:c.897+2210C>T NP_001339894.1:n.897+2210C>T
NM_001393654.1:c.993+2210C>T NP_001380583.1:n.993+2210C>T
NM_020946.2:c.993+2210C>T NP_065997.1:n.993+2210C>T
NM_001400446.1:c.903+2210C>T NP_001387375.1:n.903+2210C>T
NM_001400449.1:c.897+2210C>T NP_001387378.1:n.897+2210C>T
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