Canonical Allele Identifier: CA618011123

Gene: AP4E1

Linked Data

• dbSNP Id: rs1206780138
• gnomAD v2: 15-51289484-A-G
• gnomAD v4: 15-50997287-A-G
• MyVariant Identifiers: chr15:g.51289484A>G (hg19) ; chr15:g.50997287A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50997287A>G , CM000677.2:g.50997287A>G	GRCh38
NC_000015.9:g.51289484A>G , CM000677.1:g.51289484A>G	GRCh37
NC_000015.8:g.49076776A>G	NCBI36
NG_031875.1:g.93616A>G
NG_031875.2:g.93616A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261842.10:c.2347-39A>G MANE Select	ENSP00000261842.5:n.2347-39A>G
ENST00000261842.9:c.2347-39A>G	ENSP00000261842.5:n.2347-39A>G
ENST00000558439.5:c.*1471-39A>G	ENSP00000452712.1:n.*1471-39A>G
ENST00000560508.1:c.2122-39A>G	ENSP00000452976.1:n.2122-39A>G
ENST00000561393.5:c.*1391-39A>G	ENSP00000452711.1:n.*1391-39A>G
NM_001252127.1:c.2122-39A>G	NP_001239056.1:n.2122-39A>G
NM_007347.4:c.2347-39A>G	NP_031373.2:n.2347-39A>G
XM_005254264.2:c.2122-39A>G	XP_005254321.1:n.2122-39A>G
XM_006720447.2:c.2122-39A>G	XP_006720510.1:n.2122-39A>G
XM_011521408.1:c.2167-39A>G	XP_011519710.1:n.2167-39A>G
XM_011521409.1:c.997-39A>G	XP_011519711.1:n.997-39A>G
XM_005254264.4:c.2122-39A>G	XP_005254321.1:n.2122-39A>G
XM_006720447.4:c.2122-39A>G	XP_006720510.1:n.2122-39A>G
XM_017022042.2:c.1465-39A>G	XP_016877531.1:n.1465-39A>G
XR_001751183.1:n.2454-39A>G
XR_001751184.1:n.2330-39A>G
NM_007347.5:c.2347-39A>G MANE Select	NP_031373.2:n.2347-39A>G
NM_001252127.2:c.2122-39A>G	NP_001239056.1:n.2122-39A>G