Canonical Allele Identifier: CA392419893

Gene: AP4E1

Linked Data

• gnomAD v4: 15-50997383-G-A
• MyVariant Identifiers: chr15:g.51289580G>A (hg19) ; chr15:g.50997383G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50997383G>A , CM000677.2:g.50997383G>A	GRCh38
NC_000015.9:g.51289580G>A , CM000677.1:g.51289580G>A	GRCh37
NC_000015.8:g.49076872G>A	NCBI36
NG_031875.1:g.93712G>A
NG_031875.2:g.93712G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261842.10:c.2404G>A MANE Select	ENSP00000261842.5:p.Ala802Thr
ENST00000261842.9:c.2404G>A	ENSP00000261842.5:p.Ala802Thr
ENST00000558439.5:c.*1528G>A	ENSP00000452712.1:n.*1528G>A
ENST00000560508.1:c.2179G>A	ENSP00000452976.1:p.Ala727Thr
ENST00000561393.5:c.*1448G>A	ENSP00000452711.1:n.*1448G>A
NM_001252127.1:c.2179G>A	NP_001239056.1:p.Ala727Thr
NM_007347.4:c.2404G>A	NP_031373.2:p.Ala802Thr
XM_005254264.2:c.2179G>A	XP_005254321.1:p.Ala727Thr
XM_006720447.2:c.2179G>A	XP_006720510.1:p.Ala727Thr
XM_011521408.1:c.2224G>A	XP_011519710.1:p.Ala742Thr
XM_011521409.1:c.1054G>A	XP_011519711.1:p.Ala352Thr
XM_005254264.4:c.2179G>A	XP_005254321.1:p.Ala727Thr
XM_006720447.4:c.2179G>A	XP_006720510.1:p.Ala727Thr
XM_017022042.2:c.1522G>A	XP_016877531.1:p.Ala508Thr
XR_001751183.1:n.2511G>A
XR_001751184.1:n.2387G>A
NM_007347.5:c.2404G>A MANE Select	NP_031373.2:p.Ala802Thr
NM_001252127.2:c.2179G>A	NP_001239056.1:p.Ala727Thr