Canonical Allele Identifier: CA12636468

Gene: AP4M1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100103241A>G , CM000669.2:g.100103241A>G	GRCh38
NC_000007.13:g.99700864A>G , CM000669.1:g.99700864A>G	GRCh37
NC_000007.12:g.99538800A>G	NCBI36
NG_016312.1:g.6735A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004722.4:c.352-168A>G MANE Select	NP_004713.2:n.352-168A>G
ENST00000359593.9:c.352-168A>G MANE Select	ENSP00000352603.4:n.352-168A>G
NM_001363671.1:c.373-168A>G	NP_001350600.1:n.373-168A>G
NM_001363671.2:c.373-168A>G	NP_001350600.1:n.373-168A>G
NM_004722.3:c.352-168A>G	NP_004713.2:n.352-168A>G
ENST00000359593.8:c.352-168A>G	ENSP00000352603.4:n.352-168A>G
ENST00000394061.7:c.*305-168A>G	ENSP00000377625.3:n.*305-168A>G
ENST00000416938.5:c.308-168A>G
ENST00000421755.5:c.352-168A>G	ENSP00000412185.1:n.352-168A>G
ENST00000422582.5:c.-33-168A>G	ENSP00000406676.1:n.-33-168A>G
ENST00000429084.5:c.373-168A>G	ENSP00000403663.1:n.373-168A>G
ENST00000438383.5:c.148-168A>G	ENSP00000401613.1:n.148-168A>G
ENST00000439416.5:c.220-168A>G	ENSP00000414286.1:n.220-168A>G
ENST00000445208.5:c.255-168A>G	ENSP00000400598.1:n.255-168A>G
ENST00000445295.2:c.352-168A>G	ENSP00000393723.2:n.352-168A>G
ENST00000446007.5:c.352-168A>G	ENSP00000396928.1:n.352-168A>G
ENST00000463195.5:n.426-168A>G
ENST00000478501.5:n.856-168A>G
ENST00000495154.1:n.526A>G
ENST00000495154.2:n.526A>G
ENST00000713591.1:c.352-168A>G	ENSP00000518888.1:n.352-168A>G
XM_005250689.3:c.373-168A>G	XP_005250746.1:n.373-168A>G
XM_005250689.4:c.373-168A>G	XP_005250746.1:n.373-168A>G
XM_005250690.3:c.148-168A>G	XP_005250747.1:n.148-168A>G
XM_005250690.4:c.148-168A>G	XP_005250747.1:n.148-168A>G
XM_006716175.2:c.373-168A>G	XP_006716238.1:n.373-168A>G
XM_006716175.4:c.373-168A>G	XP_006716238.1:n.373-168A>G
XM_011516685.1:c.373-168A>G	XP_011514987.1:n.373-168A>G
XM_011516686.1:c.-33-168A>G	XP_011514988.1:n.-33-168A>G
XM_011516687.1:c.-257-168A>G	XP_011514989.1:n.-257-168A>G
XM_017012790.2:c.-33-168A>G	XP_016868279.1:n.-33-168A>G
XM_017012791.2:c.-257-168A>G	XP_016868280.1:n.-257-168A>G
XM_024446995.1:c.352-168A>G	XP_024302763.1:n.352-168A>G
XM_024446996.1:c.-257-168A>G	XP_024302764.1:n.-257-168A>G