Canonical Allele Identifier: CA13058206
Gene: DENND1A HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.123392075C>T , CM000671.2:g.123392075C>T GRCh38
NC_000009.11:g.126154354C>T , CM000671.1:g.126154354C>T GRCh37
NC_000009.10:g.125194175C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000394215.7:c.1632-4217G>A MANE Select ENSP00000377763.4:n.1632-4217G>A
ENST00000373624.6:c.1578-8162G>A ENSP00000362727.2:n.1578-8162G>A
ENST00000394219.7:c.1278-8162G>A ENSP00000377766.4:n.1278-8162G>A
ENST00000473039.5:n.1441-4217G>A
NM_020946.1:c.1578-8162G>A NP_065997.1:n.1578-8162G>A
XM_005252109.2:c.1632-4217G>A XP_005252166.1:n.1632-4217G>A
XM_005252111.3:c.1623-8162G>A XP_005252168.1:n.1623-8162G>A
XM_006717195.2:c.1623-4217G>A XP_006717258.1:n.1623-4217G>A
XM_011518882.1:c.1677-4217G>A XP_011517184.1:n.1677-4217G>A
XM_011518883.1:c.1620-4217G>A XP_011517185.1:n.1620-4217G>A
XM_011518884.1:c.1590-4217G>A XP_011517186.1:n.1590-4217G>A
XM_011518885.1:c.1569-4217G>A XP_011517187.1:n.1569-4217G>A
XM_011518886.1:c.1677-8162G>A XP_011517188.1:n.1677-8162G>A
XR_929829.1:n.2873-8162G>A
XR_929830.1:n.2816-8162G>A
NM_001352964.1:c.1632-4217G>A NP_001339893.1:n.1632-4217G>A
NM_001352965.1:c.1482-4217G>A NP_001339894.1:n.1482-4217G>A
XM_005252111.4:c.1623-8162G>A XP_005252168.1:n.1623-8162G>A
XM_006717195.4:c.1623-4217G>A XP_006717258.1:n.1623-4217G>A
XM_011518882.3:c.1677-4217G>A XP_011517184.1:n.1677-4217G>A
XM_011518883.3:c.1620-4217G>A XP_011517185.1:n.1620-4217G>A
XM_011518885.3:c.1569-4217G>A XP_011517187.1:n.1569-4217G>A
XM_011518886.3:c.1677-8162G>A XP_011517188.1:n.1677-8162G>A
XM_017014948.2:c.1578-4217G>A XP_016870437.1:n.1578-4217G>A
XM_017014949.2:c.1551-4217G>A XP_016870438.1:n.1551-4217G>A
XM_017014950.2:c.1497-4217G>A XP_016870439.1:n.1497-4217G>A
XM_017014951.2:c.1482-4217G>A XP_016870440.1:n.1482-4217G>A
XM_017014952.2:c.855-4217G>A XP_016870441.1:n.855-4217G>A
XM_024447621.1:c.1536-4217G>A XP_024303389.1:n.1536-4217G>A
XM_024447622.1:c.1542-4217G>A XP_024303390.1:n.1542-4217G>A
XM_024447623.1:c.1044-4217G>A XP_024303391.1:n.1044-4217G>A
XR_929829.2:n.2882-8162G>A
XR_929830.3:n.2825-8162G>A
NM_001352964.2:c.1632-4217G>A MANE Select NP_001339893.1:n.1632-4217G>A
NM_001352965.2:c.1482-4217G>A NP_001339894.1:n.1482-4217G>A
NM_001393654.1:c.1578-4217G>A NP_001380583.1:n.1578-4217G>A
NM_020946.2:c.1578-8162G>A NP_065997.1:n.1578-8162G>A
NM_001400449.1:c.1482-4217G>A NP_001387378.1:n.1482-4217G>A
Search 100 bp 5'
Search 100 bp 3'