Canonical Allele Identifier: CA392419894

Gene: AP4E1

Linked Data

• MyVariant Identifiers: chr15:g.51289581C>A (hg19) ; chr15:g.50997384C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50997384C>A , CM000677.2:g.50997384C>A	GRCh38
NC_000015.9:g.51289581C>A , CM000677.1:g.51289581C>A	GRCh37
NC_000015.8:g.49076873C>A	NCBI36
NG_031875.1:g.93713C>A
NG_031875.2:g.93713C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000261842.10:c.2405C>A MANE Select	ENSP00000261842.5:p.Ala802Asp
ENST00000261842.9:c.2405C>A	ENSP00000261842.5:p.Ala802Asp
ENST00000558439.5:c.*1529C>A	ENSP00000452712.1:n.*1529C>A
ENST00000560508.1:c.2180C>A	ENSP00000452976.1:p.Ala727Asp
ENST00000561393.5:c.*1449C>A	ENSP00000452711.1:n.*1449C>A
NM_001252127.1:c.2180C>A	NP_001239056.1:p.Ala727Asp
NM_007347.4:c.2405C>A	NP_031373.2:p.Ala802Asp
XM_005254264.2:c.2180C>A	XP_005254321.1:p.Ala727Asp
XM_006720447.2:c.2180C>A	XP_006720510.1:p.Ala727Asp
XM_011521408.1:c.2225C>A	XP_011519710.1:p.Ala742Asp
XM_011521409.1:c.1055C>A	XP_011519711.1:p.Ala352Asp
XM_005254264.4:c.2180C>A	XP_005254321.1:p.Ala727Asp
XM_006720447.4:c.2180C>A	XP_006720510.1:p.Ala727Asp
XM_017022042.2:c.1523C>A	XP_016877531.1:p.Ala508Asp
XR_001751183.1:n.2512C>A
XR_001751184.1:n.2388C>A
NM_007347.5:c.2405C>A MANE Select	NP_031373.2:p.Ala802Asp
NM_001252127.2:c.2180C>A	NP_001239056.1:p.Ala727Asp