Canonical Allele Identifier: CA163213090

Gene: AP4M1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.100102430_100102431insC , CM000669.2:g.100102430_100102431insC	GRCh38
NC_000007.13:g.99700053_99700054insC , CM000669.1:g.99700053_99700054insC	GRCh37
NC_000007.12:g.99537989_99537990insC	NCBI36
NG_016312.1:g.5924_5925insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445295.2:c.148-245_148-244insC	ENSP00000393723.2:n.148-245_148-244insC
ENST00000495154.2:n.308+37_308+38insC
ENST00000713591.1:c.148-245_148-244insC	ENSP00000518888.1:n.148-245_148-244insC
ENST00000359593.9:c.148-245_148-244insC MANE Select	ENSP00000352603.4:n.148-245_148-244insC
ENST00000359593.8:c.148-245_148-244insC	ENSP00000352603.4:n.148-245_148-244insC
ENST00000394061.7:c.*100+37_*100+38insC	ENSP00000377625.3:n.*100+37_*100+38insC
ENST00000416938.5:c.104-245_104-244insC
ENST00000421755.5:c.148-245_148-244insC	ENSP00000412185.1:n.148-245_148-244insC
ENST00000422582.5:c.-238+37_-238+38insC	ENSP00000406676.1:n.-238+37_-238+38insC
ENST00000429084.5:c.169-245_169-244insC	ENSP00000403663.1:n.169-245_169-244insC
ENST00000438383.5:c.147+462_147+463insC	ENSP00000401613.1:n.147+462_147+463insC
ENST00000439416.5:c.148-245_148-244insC	ENSP00000414286.1:n.148-245_148-244insC
ENST00000445208.5:c.148-245_148-244insC	ENSP00000400598.1:n.148-245_148-244insC
ENST00000446007.5:c.148-245_148-244insC	ENSP00000396928.1:n.148-245_148-244insC
ENST00000463195.5:n.222-245_222-244insC
ENST00000478501.5:n.651+37_651+38insC
ENST00000495154.1:n.308+37_308+38insC
NM_004722.3:c.148-245_148-244insC	NP_004713.2:n.148-245_148-244insC
XM_005250689.3:c.169-245_169-244insC	XP_005250746.1:n.169-245_169-244insC
XM_005250690.3:c.147+462_147+463insC	XP_005250747.1:n.147+462_147+463insC
XM_006716175.2:c.169-245_169-244insC	XP_006716238.1:n.169-245_169-244insC
XM_011516685.1:c.169-245_169-244insC	XP_011514987.1:n.169-245_169-244insC
XM_011516686.1:c.-238+37_-238+38insC	XP_011514988.1:n.-238+37_-238+38insC
NM_001363671.1:c.169-245_169-244insC	NP_001350600.1:n.169-245_169-244insC
XM_005250689.4:c.169-245_169-244insC	XP_005250746.1:n.169-245_169-244insC
XM_005250690.4:c.147+462_147+463insC	XP_005250747.1:n.147+462_147+463insC
XM_006716175.4:c.169-245_169-244insC	XP_006716238.1:n.169-245_169-244insC
XM_017012790.2:c.-238+37_-238+38insC	XP_016868279.1:n.-238+37_-238+38insC
XM_017012791.2:c.-258+462_-258+463insC	XP_016868280.1:n.-258+462_-258+463insC
XM_024446995.1:c.148-245_148-244insC	XP_024302763.1:n.148-245_148-244insC
XM_024446996.1:c.-462+37_-462+38insC	XP_024302764.1:n.-462+37_-462+38insC
NM_004722.4:c.148-245_148-244insC MANE Select	NP_004713.2:n.148-245_148-244insC
NM_001363671.2:c.169-245_169-244insC	NP_001350600.1:n.169-245_169-244insC