Canonical Allele Identifier: CA2176672554

Gene: AP4E1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50997386A= , CM000677.2:g.50997386A=	GRCh38
NC_000015.9:g.51289583A= , CM000677.1:g.51289583A=	GRCh37
NC_000015.8:g.49076875A=	NCBI36
NG_031875.1:g.93715A=
NG_031875.2:g.93715A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261842.10:c.2407A= MANE Select	ENSP00000261842.5:p.Lys803=
ENST00000261842.9:c.2407A=	ENSP00000261842.5:p.Lys803=
ENST00000558439.5:c.*1531A=	ENSP00000452712.1:n.*1531A=
ENST00000560508.1:c.2182A=	ENSP00000452976.1:p.Lys728=
ENST00000561393.5:c.*1451A=	ENSP00000452711.1:n.*1451A=
NM_001252127.1:c.2182A=	NP_001239056.1:p.Lys728=
NM_007347.4:c.2407A=	NP_031373.2:p.Lys803=
XM_005254264.2:c.2182A=	XP_005254321.1:p.Lys728=
XM_006720447.2:c.2182A=	XP_006720510.1:p.Lys728=
XM_011521408.1:c.2227A=	XP_011519710.1:p.Lys743=
XM_011521409.1:c.1057A=	XP_011519711.1:p.Lys353=
XM_005254264.4:c.2182A=	XP_005254321.1:p.Lys728=
XM_006720447.4:c.2182A=	XP_006720510.1:p.Lys728=
XM_017022042.2:c.1525A=	XP_016877531.1:p.Lys509=
XR_001751183.1:n.2514A=
XR_001751184.1:n.2390A=
NM_007347.5:c.2407A= MANE Select	NP_031373.2:p.Lys803=
NM_001252127.2:c.2182A=	NP_001239056.1:p.Lys728=