Canonical Allele Identifier: CA1729350937

Gene: AP4M1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100106104A= , CM000669.2:g.100106104A=	GRCh38
NC_000007.13:g.99703727A= , CM000669.1:g.99703727A=	GRCh37
NC_000007.12:g.99541663A=	NCBI36
NG_016312.1:g.9598A=
NG_029454.1:g.18755T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004722.4:c.974+101A= MANE Select	NP_004713.2:n.974+101A=
ENST00000359593.9:c.974+101A= MANE Select	ENSP00000352603.4:n.974+101A=
NM_001363671.1:c.995+101A=	NP_001350600.1:n.995+101A=
NM_001363671.2:c.995+101A=	NP_001350600.1:n.995+101A=
NM_004722.3:c.974+101A=	NP_004713.2:n.974+101A=
ENST00000359593.8:c.974+101A=	ENSP00000352603.4:n.974+101A=
ENST00000416938.5:c.863+101A=
ENST00000421755.5:c.974+101A=	ENSP00000412185.1:n.974+101A=
ENST00000422582.5:c.590+101A=	ENSP00000406676.1:n.590+101A=
ENST00000429084.5:c.995+101A=	ENSP00000403663.1:n.995+101A=
ENST00000438383.5:c.770+101A=	ENSP00000401613.1:n.770+101A=
ENST00000445208.5:c.*583+101A=	ENSP00000400598.1:n.*583+101A=
ENST00000445295.1:c.151+101A=
ENST00000445295.2:c.974+101A=	ENSP00000393723.2:n.974+101A=
ENST00000446007.5:c.*196+101A=	ENSP00000396928.1:n.*196+101A=
ENST00000450807.5:c.230+101A=	ENSP00000391585.1:n.230+101A=
ENST00000489387.1:n.128A=
ENST00000495154.2:n.1233+101A=
ENST00000713591.1:c.974+101A=	ENSP00000518888.1:n.974+101A=
XM_005250689.3:c.995+101A=	XP_005250746.1:n.995+101A=
XM_005250689.4:c.995+101A=	XP_005250746.1:n.995+101A=
XM_005250690.3:c.770+101A=	XP_005250747.1:n.770+101A=
XM_005250690.4:c.770+101A=	XP_005250747.1:n.770+101A=
XM_006716175.2:c.995+101A=	XP_006716238.1:n.995+101A=
XM_006716175.4:c.995+101A=	XP_006716238.1:n.995+101A=
XM_011516685.1:c.995+101A=	XP_011514987.1:n.995+101A=
XM_011516686.1:c.590+101A=	XP_011514988.1:n.590+101A=
XM_011516687.1:c.299+101A=	XP_011514989.1:n.299+101A=
XM_017012790.2:c.590+101A=	XP_016868279.1:n.590+101A=
XM_017012791.2:c.299+101A=	XP_016868280.1:n.299+101A=
XM_024446995.1:c.974+101A=	XP_024302763.1:n.974+101A=
XM_024446996.1:c.299+101A=	XP_024302764.1:n.299+101A=