Canonical Allele Identifier: CA2176636414

Gene: AP4E1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50928858A= , CM000677.2:g.50928858A=	GRCh38
NC_000015.9:g.51221055A= , CM000677.1:g.51221055A=	GRCh37
NC_000015.8:g.49008347A=	NCBI36
NG_031875.1:g.25187A=
NG_031875.2:g.25187A=

Transcript Alleles

HGVS	Amino-acid Change
NM_007347.5:c.543-151A= MANE Select	NP_031373.2:n.543-151A=
ENST00000261842.10:c.543-151A= MANE Select	ENSP00000261842.5:n.543-151A=
NM_001252127.1:c.318-151A=	NP_001239056.1:n.318-151A=
NM_001252127.2:c.318-151A=	NP_001239056.1:n.318-151A=
NM_007347.4:c.543-151A=	NP_031373.2:n.543-151A=
ENST00000261842.9:c.543-151A=	ENSP00000261842.5:n.543-151A=
ENST00000558439.5:c.543-151A=	ENSP00000452712.1:n.543-151A=
ENST00000560508.1:c.318-151A=	ENSP00000452976.1:n.318-151A=
ENST00000561393.5:c.318-151A=	ENSP00000452711.1:n.318-151A=
ENST00000561441.5:c.543-151A=	ENSP00000453112.1:n.543-151A=
XM_005254264.2:c.318-151A=	XP_005254321.1:n.318-151A=
XM_005254264.4:c.318-151A=	XP_005254321.1:n.318-151A=
XM_006720447.2:c.318-151A=	XP_006720510.1:n.318-151A=
XM_006720447.4:c.318-151A=	XP_006720510.1:n.318-151A=
XM_011521408.1:c.363-151A=	XP_011519710.1:n.363-151A=
XM_011521409.1:c.-898-151A=	XP_011519711.1:n.-898-151A=
XM_017022042.2:c.-428-151A=	XP_016877531.1:n.-428-151A=
XR_001751183.1:n.650-151A=
XR_001751184.1:n.650-151A=
XR_001751185.1:n.650-151A=