Canonical Allele Identifier: CA2579700832

Gene: AIFM1 RAB33A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.130138523A>G , CM000685.2:g.130138523A>G	GRCh38
NC_000023.10:g.129272498A>G , CM000685.1:g.129272498A>G	GRCh37
NC_000023.9:g.129100179A>G	NCBI36
NG_013217.1:g.32311T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287295.8:c.967+70T>C (AIFM1) MANE Select	ENSP00000287295.3:n.967+70T>C
ENST00000319908.8:c.964+70T>C (AIFM1)	ENSP00000315122.4:n.964+70T>C
ENST00000416073.7:c.961+70T>C (AIFM1)	ENSP00000402535.3:n.961+70T>C
ENST00000533719.2:n.759+70T>C (AIFM1)
ENST00000535724.6:c.967+70T>C (AIFM1)	ENSP00000446113.2:n.967+70T>C
ENST00000674546.1:c.967+70T>C (AIFM1)	ENSP00000501950.1:n.967+70T>C
ENST00000674555.1:c.*702+70T>C (AIFM1)	ENSP00000502183.1:n.*702+70T>C
ENST00000674722.1:c.*135+70T>C (AIFM1)	ENSP00000501693.1:n.*135+70T>C
ENST00000674957.1:c.668+70T>C (AIFM1)
ENST00000674997.1:c.824+70T>C (AIFM1)	ENSP00000502124.1:n.824+70T>C
ENST00000675037.1:c.967+70T>C (AIFM1)	ENSP00000501724.1:n.967+70T>C
ENST00000675050.1:c.955+70T>C (AIFM1)	ENSP00000502606.1:n.955+70T>C
ENST00000675092.1:c.967+70T>C (AIFM1)	ENSP00000501772.1:n.967+70T>C
ENST00000675111.1:n.892+70T>C (AIFM1)
ENST00000675240.1:c.967+70T>C (AIFM1)	ENSP00000501907.1:n.967+70T>C
ENST00000675427.1:c.967+70T>C (AIFM1)	ENSP00000501880.1:n.967+70T>C
ENST00000675774.1:c.*821T>C (AIFM1)	ENSP00000502690.1:n.*821T>C
ENST00000675857.1:c.961+70T>C (AIFM1)	ENSP00000502721.1:n.961+70T>C
ENST00000676048.1:n.4089+70T>C (AIFM1)
ENST00000676144.1:c.742+70T>C (AIFM1)
ENST00000676229.1:c.955+70T>C (AIFM1)	ENSP00000502184.1:n.955+70T>C
ENST00000676328.1:c.964+70T>C (AIFM1)	ENSP00000502068.1:n.964+70T>C
ENST00000676436.1:c.961+70T>C (AIFM1)	ENSP00000502669.1:n.961+70T>C
ENST00000287295.7:c.967+70T>C (AIFM1)	ENSP00000287295.3:n.967+70T>C
ENST00000319908.7:c.955+70T>C (AIFM1)	ENSP00000315122.3:n.955+70T>C
ENST00000346424.6:c.107-1338T>C (AIFM1)	ENSP00000316320.3:n.107-1338T>C
ENST00000416073.6:c.967+70T>C (AIFM1)	ENSP00000402535.2:n.967+70T>C
ENST00000527892.5:c.*692+70T>C (AIFM1)	ENSP00000435955.1:n.*692+70T>C
ENST00000533719.1:n.670+70T>C (AIFM1)
ENST00000535724.5:c.967+70T>C (AIFM1)	ENSP00000446113.2:n.967+70T>C
NM_001130847.3:c.967+70T>C (AIFM1)	NP_001124319.1:n.967+70T>C
NM_004208.3:c.967+70T>C (AIFM1)	NP_004199.1:n.967+70T>C
NM_145812.2:c.955+70T>C (AIFM1)	NP_665811.1:n.955+70T>C
NM_145813.2:c.107-1338T>C (AIFM1)	NP_665812.1:n.107-1338T>C
NR_132647.1:n.1055+70T>C (AIFM1)
XM_017029963.2:c.30+21138A>G (RAB33A)	XP_016885452.1:n.30+21138A>G
NM_004208.4:c.967+70T>C (AIFM1) MANE Select	NP_004199.1:n.967+70T>C
NM_001130847.4:c.967+70T>C (AIFM1)	NP_001124319.1:n.967+70T>C
NM_145812.3:c.955+70T>C (AIFM1)	NP_665811.1:n.955+70T>C
NR_132647.2:n.1009+70T>C (AIFM1)