Canonical Allele Identifier: CA341713803

Gene: AP4B1 AP4B1-AS1

Linked Data

• dbSNP Id: rs1162959753
• gnomAD v3: 1-113900308-A-G
• gnomAD v4: 1-113900308-A-G
• MyVariant Identifiers: chr1:g.114442930A>G (hg19) ; chr1:g.113900308A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.113900308A>G , CM000663.2:g.113900308A>G	GRCh38
NC_000001.10:g.114442930A>G , CM000663.1:g.114442930A>G	GRCh37
NC_000001.9:g.114244453A>G	NCBI36
NG_031901.1:g.9812T>C
NG_057565.1:g.690A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369564.6:c.485T>C (AP4B1)	ENSP00000358577.2:p.Leu162Pro
ENST00000369567.6:c.206T>C (AP4B1)	ENSP00000358580.1:p.Leu69Pro
ENST00000369571.3:c.710T>C (AP4B1)	ENSP00000358584.3:p.Leu237Pro
ENST00000432415.6:c.206T>C (AP4B1)	ENSP00000393622.2:p.Leu69Pro
ENST00000460653.2:c.710T>C (AP4B1)	ENSP00000518881.1:p.Leu237Pro
ENST00000484201.6:c.485T>C (AP4B1)	ENSP00000518883.1:p.Leu162Pro
ENST00000489092.6:c.*378T>C (AP4B1)	ENSP00000518884.1:n.*378T>C
ENST00000489499.6:c.*52T>C (AP4B1)	ENSP00000518882.1:n.*52T>C
ENST00000713588.1:c.710T>C (AP4B1)	ENSP00000518880.1:p.Leu237Pro
ENST00000713590.1:c.710T>C (AP4B1)	ENSP00000518886.1:p.Leu237Pro
ENST00000369569.6:c.710T>C (AP4B1) MANE Select	ENSP00000358582.1:p.Leu237Pro
ENST00000256658.8:c.710T>C (AP4B1)	ENSP00000256658.4:p.Leu237Pro
ENST00000369564.5:c.485T>C (AP4B1)	ENSP00000358577.1:p.Leu162Pro
ENST00000369567.5:c.206T>C (AP4B1)	ENSP00000358580.1:p.Leu69Pro
ENST00000369569.5:c.710T>C (AP4B1)	ENSP00000358582.1:p.Leu237Pro
ENST00000369571.2:c.710T>C (AP4B1)	ENSP00000358584.2:p.Leu237Pro
ENST00000432415.5:c.206T>C (AP4B1)	ENSP00000393622.1:p.Leu69Pro
ENST00000484201.5:n.676T>C (AP4B1)
ENST00000489092.5:n.709T>C (AP4B1)
ENST00000489499.5:n.678T>C (AP4B1)
NM_001253852.1:c.710T>C (AP4B1)	NP_001240781.1:p.Leu237Pro
NM_001253852.2:c.710T>C (AP4B1)	NP_001240781.1:p.Leu237Pro
NM_001253853.1:c.413T>C (AP4B1)	NP_001240782.1:p.Leu138Pro
NM_001253853.2:c.413T>C (AP4B1)	NP_001240782.1:p.Leu138Pro
NM_001308312.1:c.206T>C (AP4B1)	NP_001295241.1:p.Leu69Pro
NM_006594.3:c.710T>C (AP4B1)	NP_006585.2:p.Leu237Pro
NM_006594.4:c.710T>C (AP4B1)	NP_006585.2:p.Leu237Pro
NR_037864.1:n.805A>G (AP4B1-AS1)
NR_125965.1:n.973A>G (AP4B1-AS1)
XM_005270381.2:c.710T>C (AP4B1)	XP_005270438.1:p.Leu237Pro
XM_005270382.3:c.710T>C (AP4B1)	XP_005270439.1:p.Leu237Pro
XM_011540523.1:c.485T>C (AP4B1)	XP_011538825.1:p.Leu162Pro
XM_011540524.1:c.485T>C (AP4B1)	XP_011538826.1:p.Leu162Pro
XM_011540525.1:c.431T>C (AP4B1)	XP_011538827.1:p.Leu144Pro
XM_011540527.1:c.92T>C (AP4B1)	XP_011538829.1:p.Leu31Pro
XR_246227.1:n.892T>C (AP4B1)
XR_246228.2:n.892T>C (AP4B1)
XM_011540523.3:c.485T>C (AP4B1)	XP_011538825.1:p.Leu162Pro
XM_011540525.3:c.431T>C (AP4B1)	XP_011538827.1:p.Leu144Pro
XM_017000089.2:c.710T>C (AP4B1)	XP_016855578.1:p.Leu237Pro
XM_017000090.1:c.206T>C (AP4B1)	XP_016855579.1:p.Leu69Pro
XM_017000091.2:c.431T>C (AP4B1)	XP_016855580.1:p.Leu144Pro
XM_017000092.2:c.-535T>C (AP4B1)	XP_016855581.1:n.-535T>C
XM_017000093.2:c.710T>C (AP4B1)	XP_016855582.1:p.Leu237Pro
XM_024452422.1:c.431T>C (AP4B1)	XP_024308190.1:p.Leu144Pro
XM_024452423.1:c.710T>C (AP4B1)	XP_024308191.1:p.Leu237Pro
XM_024452435.1:c.485T>C (AP4B1)	XP_024308203.1:p.Leu162Pro
XM_024452441.1:c.206T>C (AP4B1)	XP_024308209.1:p.Leu69Pro
XR_001736928.2:n.912T>C (AP4B1)
XR_001736930.2:n.912T>C (AP4B1)
XR_002958805.1:n.912T>C (AP4B1)
XR_002958806.1:n.912T>C (AP4B1)
XR_002958807.1:n.792T>C (AP4B1)
NM_001253852.3:c.710T>C (AP4B1) MANE Select	NP_001240781.1:p.Leu237Pro
NM_001253853.3:c.413T>C (AP4B1)	NP_001240782.1:p.Leu138Pro
NM_001308312.2:c.206T>C (AP4B1)	NP_001295241.1:p.Leu69Pro
NM_006594.5:c.710T>C (AP4B1)	NP_006585.2:p.Leu237Pro