Canonical Allele Identifier: CA1189947493
Gene: AP4B1 HGNC NCBI
AP4B1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.113899994_113900002delinsCGTTCACCA , CM000663.2:g.113899994_113900002delinsCGTTCACCA GRCh38
NC_000001.10:g.114442616_114442624delinsCGTTCACCA , CM000663.1:g.114442616_114442624delinsCGTTCACCA GRCh37
NC_000001.9:g.114244139_114244147delinsCGTTCACCA NCBI36
NG_031901.1:g.10118_10126delinsTGGTGAACG
NG_057565.1:g.376_384delinsCGTTCACCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369564.6:c.791_799delinsTGGTGAACG (AP4B1) ENSP00000358577.2:p.Leu264=
ENST00000369567.6:c.512_520delinsTGGTGAACG (AP4B1) ENSP00000358580.1:p.Leu171=
ENST00000369571.3:c.1016_1024delinsTGGTGAACG (AP4B1) ENSP00000358584.3:p.Leu339=
ENST00000432415.6:c.512_520delinsTGGTGAACG (AP4B1) ENSP00000393622.2:p.Leu171=
ENST00000460653.2:c.1016_1024delinsTGGTGAACG (AP4B1) ENSP00000518881.1:p.Leu339=
ENST00000484201.6:c.523+268_523+276delinsTGGTGAACG (AP4B1) ENSP00000518883.1:n.523+268_523+276delinsTGGTGAACG
ENST00000489499.6:c.*358_*366delinsTGGTGAACG (AP4B1) ENSP00000518882.1:n.*358_*366delinsTGGTGAACG
ENST00000713588.1:c.1016_1024delinsTGGTGAACG (AP4B1) ENSP00000518880.1:p.Leu339=
ENST00000713590.1:c.1016_1024delinsTGGTGAACG (AP4B1) ENSP00000518886.1:p.Leu339=
ENST00000369569.6:c.1016_1024delinsTGGTGAACG (AP4B1) MANE Select ENSP00000358582.1:p.Leu339=
ENST00000256658.8:c.1016_1024delinsTGGTGAACG (AP4B1) ENSP00000256658.4:p.Leu339=
ENST00000369564.5:c.791_799delinsTGGTGAACG (AP4B1) ENSP00000358577.1:p.Leu264=
ENST00000369567.5:c.512_520delinsTGGTGAACG (AP4B1) ENSP00000358580.1:p.Leu171=
ENST00000369569.5:c.1016_1024delinsTGGTGAACG (AP4B1) ENSP00000358582.1:p.Leu339=
ENST00000432415.5:c.512_520delinsTGGTGAACG (AP4B1) ENSP00000393622.1:p.Leu171=
ENST00000460653.1:n.7_15delinsTGGTGAACG (AP4B1)
ENST00000479285.5:n.244_252delinsTGGTGAACG (AP4B1)
ENST00000484201.5:n.714+268_714+276delinsTGGTGAACG (AP4B1)
ENST00000489499.5:n.984_992delinsTGGTGAACG (AP4B1)
NM_001253852.1:c.1016_1024delinsTGGTGAACG (AP4B1) NP_001240781.1:p.Leu339=
NM_001253852.2:c.1016_1024delinsTGGTGAACG (AP4B1) NP_001240781.1:p.Leu339=
NM_001253853.1:c.719_727delinsTGGTGAACG (AP4B1) NP_001240782.1:p.Leu240=
NM_001253853.2:c.719_727delinsTGGTGAACG (AP4B1) NP_001240782.1:p.Leu240=
NM_001308312.1:c.512_520delinsTGGTGAACG (AP4B1) NP_001295241.1:p.Leu171=
NM_006594.3:c.1016_1024delinsTGGTGAACG (AP4B1) NP_006585.2:p.Leu339=
NM_006594.4:c.1016_1024delinsTGGTGAACG (AP4B1) NP_006585.2:p.Leu339=
NR_037864.1:n.491_499delinsCGTTCACCA (AP4B1-AS1)
NR_125965.1:n.659_667delinsCGTTCACCA (AP4B1-AS1)
XM_005270381.2:c.1016_1024delinsTGGTGAACG (AP4B1) XP_005270438.1:p.Leu339=
XM_005270382.3:c.1016_1024delinsTGGTGAACG (AP4B1) XP_005270439.1:p.Leu339=
XM_011540523.1:c.791_799delinsTGGTGAACG (AP4B1) XP_011538825.1:p.Leu264=
XM_011540524.1:c.791_799delinsTGGTGAACG (AP4B1) XP_011538826.1:p.Leu264=
XM_011540525.1:c.737_745delinsTGGTGAACG (AP4B1) XP_011538827.1:p.Leu246=
XM_011540527.1:c.398_406delinsTGGTGAACG (AP4B1) XP_011538829.1:p.Leu133=
XR_246227.1:n.1198_1206delinsTGGTGAACG (AP4B1)
XR_246228.2:n.1198_1206delinsTGGTGAACG (AP4B1)
XM_011540523.3:c.791_799delinsTGGTGAACG (AP4B1) XP_011538825.1:p.Leu264=
XM_011540525.3:c.737_745delinsTGGTGAACG (AP4B1) XP_011538827.1:p.Leu246=
XM_017000089.2:c.1016_1024delinsTGGTGAACG (AP4B1) XP_016855578.1:p.Leu339=
XM_017000090.1:c.512_520delinsTGGTGAACG (AP4B1) XP_016855579.1:p.Leu171=
XM_017000091.2:c.737_745delinsTGGTGAACG (AP4B1) XP_016855580.1:p.Leu246=
XM_017000092.2:c.-229_-221delinsTGGTGAACG (AP4B1) XP_016855581.1:n.-229_-221delinsTGGTGAACG
XM_017000093.2:c.1016_1024delinsTGGTGAACG (AP4B1) XP_016855582.1:p.Leu339=
XM_024452422.1:c.737_745delinsTGGTGAACG (AP4B1) XP_024308190.1:p.Leu246=
XM_024452423.1:c.1016_1024delinsTGGTGAACG (AP4B1) XP_024308191.1:p.Leu339=
XM_024452435.1:c.791_799delinsTGGTGAACG (AP4B1) XP_024308203.1:p.Leu264=
XM_024452441.1:c.512_520delinsTGGTGAACG (AP4B1) XP_024308209.1:p.Leu171=
XR_001736928.2:n.1218_1226delinsTGGTGAACG (AP4B1)
XR_001736930.2:n.1218_1226delinsTGGTGAACG (AP4B1)
XR_002958805.1:n.1218_1226delinsTGGTGAACG (AP4B1)
XR_002958806.1:n.1218_1226delinsTGGTGAACG (AP4B1)
XR_002958807.1:n.1098_1106delinsTGGTGAACG (AP4B1)
NM_001253852.3:c.1016_1024delinsTGGTGAACG (AP4B1) MANE Select NP_001240781.1:p.Leu339=
NM_001253853.3:c.719_727delinsTGGTGAACG (AP4B1) NP_001240782.1:p.Leu240=
NM_001308312.2:c.512_520delinsTGGTGAACG (AP4B1) NP_001295241.1:p.Leu171=
NM_006594.5:c.1016_1024delinsTGGTGAACG (AP4B1) NP_006585.2:p.Leu339=