Canonical Allele Identifier: CA341710226

Gene: AP4B1 AP4B1-AS1

Linked Data

• gnomAD v4: 1-113896371-G-C
• MyVariant Identifiers: chr1:g.114438993G>C (hg19) ; chr1:g.113896371G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113896371G>C , CM000663.2:g.113896371G>C	GRCh38
NC_000001.10:g.114438993G>C , CM000663.1:g.114438993G>C	GRCh37
NC_000001.9:g.114240516G>C	NCBI36
NG_031901.1:g.13749C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.1172C>G (AP4B1)	ENSP00000358577.2:p.Ser391Trp
ENST00000369567.6:c.893C>G (AP4B1)	ENSP00000358580.1:p.Ser298Trp
ENST00000369571.3:c.1397C>G (AP4B1)	ENSP00000358584.3:p.Ser466Trp
ENST00000432415.6:c.893C>G (AP4B1)	ENSP00000393622.2:p.Ser298Trp
ENST00000460653.2:c.*467C>G (AP4B1)	ENSP00000518881.1:n.*467C>G
ENST00000484201.6:c.*147C>G (AP4B1)	ENSP00000518883.1:n.*147C>G
ENST00000489499.6:c.*739C>G (AP4B1)	ENSP00000518882.1:n.*739C>G
ENST00000713588.1:c.*508C>G (AP4B1)	ENSP00000518880.1:n.*508C>G
ENST00000713590.1:c.1397C>G (AP4B1)	ENSP00000518886.1:p.Ser466Trp
ENST00000369569.6:c.1397C>G (AP4B1) MANE Select	ENSP00000358582.1:p.Ser466Trp
ENST00000256658.8:c.1397C>G (AP4B1)	ENSP00000256658.4:p.Ser466Trp
ENST00000369567.5:c.893C>G (AP4B1)	ENSP00000358580.1:p.Ser298Trp
ENST00000369569.5:c.1397C>G (AP4B1)	ENSP00000358582.1:p.Ser466Trp
ENST00000462591.1:n.1569C>G (AP4B1)
ENST00000479285.5:n.625C>G (AP4B1)
ENST00000479801.1:n.231C>G (AP4B1)
ENST00000484201.5:n.959C>G (AP4B1)
NM_001253852.1:c.1397C>G (AP4B1)	NP_001240781.1:p.Ser466Trp
NM_001253852.2:c.1397C>G (AP4B1)	NP_001240781.1:p.Ser466Trp
NM_001253853.1:c.1100C>G (AP4B1)	NP_001240782.1:p.Ser367Trp
NM_001253853.2:c.1100C>G (AP4B1)	NP_001240782.1:p.Ser367Trp
NM_001308312.1:c.893C>G (AP4B1)	NP_001295241.1:p.Ser298Trp
NM_006594.3:c.1397C>G (AP4B1)	NP_006585.2:p.Ser466Trp
NM_006594.4:c.1397C>G (AP4B1)	NP_006585.2:p.Ser466Trp
NR_037864.1:n.247-1497G>C (AP4B1-AS1)
NR_125965.1:n.415-1497G>C (AP4B1-AS1)
XM_005270381.2:c.1199-333C>G (AP4B1)	XP_005270438.1:n.1199-333C>G
XM_011540523.1:c.1172C>G (AP4B1)	XP_011538825.1:p.Ser391Trp
XM_011540524.1:c.1172C>G (AP4B1)	XP_011538826.1:p.Ser391Trp
XM_011540525.1:c.1118C>G (AP4B1)	XP_011538827.1:p.Ser373Trp
XM_011540527.1:c.779C>G (AP4B1)	XP_011538829.1:p.Ser260Trp
XM_011540528.1:c.422C>G (AP4B1)	XP_011538830.1:p.Ser141Trp
XR_246227.1:n.1485-333C>G (AP4B1)
XM_011540523.3:c.1172C>G (AP4B1)	XP_011538825.1:p.Ser391Trp
XM_011540525.3:c.1118C>G (AP4B1)	XP_011538827.1:p.Ser373Trp
XM_017000089.2:c.1199-333C>G (AP4B1)	XP_016855578.1:n.1199-333C>G
XM_017000090.1:c.893C>G (AP4B1)	XP_016855579.1:p.Ser298Trp
XM_017000091.2:c.920-333C>G (AP4B1)	XP_016855580.1:n.920-333C>G
XM_017000092.2:c.422C>G (AP4B1)	XP_016855581.1:p.Ser141Trp
XM_024452422.1:c.1118C>G (AP4B1)	XP_024308190.1:p.Ser373Trp
XM_024452423.1:c.1199-333C>G (AP4B1)	XP_024308191.1:n.1199-333C>G
XM_024452435.1:c.974-333C>G (AP4B1)	XP_024308203.1:n.974-333C>G
XM_024452441.1:c.695-333C>G (AP4B1)	XP_024308209.1:n.695-333C>G
XR_001736928.2:n.1827C>G (AP4B1)
XR_001736930.2:n.1971C>G (AP4B1)
XR_002958805.1:n.1505-333C>G (AP4B1)
XR_002958806.1:n.1868C>G (AP4B1)
XR_002958807.1:n.1707C>G (AP4B1)
NM_001253852.3:c.1397C>G (AP4B1) MANE Select	NP_001240781.1:p.Ser466Trp
NM_001253853.3:c.1100C>G (AP4B1)	NP_001240782.1:p.Ser367Trp
NM_001308312.2:c.893C>G (AP4B1)	NP_001295241.1:p.Ser298Trp
NM_006594.5:c.1397C>G (AP4B1)	NP_006585.2:p.Ser466Trp