Canonical Allele Identifier: CA2694683707

Gene: AIFM1 RAB33A

Linked Data

• gnomAD v4: X-130139913-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.130139913G>C , CM000685.2:g.130139913G>C	GRCh38
NC_000023.10:g.129273888G>C , CM000685.1:g.129273888G>C	GRCh37
NC_000023.9:g.129101569G>C	NCBI36
NG_013217.1:g.30921C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000287295.8:c.782-42C>G (AIFM1) MANE Select	ENSP00000287295.3:n.782-42C>G
ENST00000319908.8:c.782-45C>G (AIFM1)	ENSP00000315122.4:n.782-45C>G
ENST00000416073.7:c.776-42C>G (AIFM1)	ENSP00000402535.3:n.776-42C>G
ENST00000533719.2:n.574-42C>G (AIFM1)
ENST00000535724.6:c.782-42C>G (AIFM1)	ENSP00000446113.2:n.782-42C>G
ENST00000674546.1:c.782-42C>G (AIFM1)	ENSP00000501950.1:n.782-42C>G
ENST00000674555.1:c.*517-42C>G (AIFM1)	ENSP00000502183.1:n.*517-42C>G
ENST00000674722.1:c.697-42C>G (AIFM1)	ENSP00000501693.1:n.697-42C>G
ENST00000674957.1:c.483-42C>G (AIFM1)
ENST00000674997.1:c.639-42C>G (AIFM1)	ENSP00000502124.1:n.639-42C>G
ENST00000675037.1:c.782-42C>G (AIFM1)	ENSP00000501724.1:n.782-42C>G
ENST00000675050.1:c.770-42C>G (AIFM1)	ENSP00000502606.1:n.770-42C>G
ENST00000675092.1:c.782-42C>G (AIFM1)	ENSP00000501772.1:n.782-42C>G
ENST00000675111.1:n.707-42C>G (AIFM1)
ENST00000675240.1:c.782-42C>G (AIFM1)	ENSP00000501907.1:n.782-42C>G
ENST00000675427.1:c.782-42C>G (AIFM1)	ENSP00000501880.1:n.782-42C>G
ENST00000675774.1:c.*566-42C>G (AIFM1)	ENSP00000502690.1:n.*566-42C>G
ENST00000675857.1:c.776-42C>G (AIFM1)	ENSP00000502721.1:n.776-42C>G
ENST00000676048.1:n.3904-42C>G (AIFM1)
ENST00000676144.1:c.557-42C>G (AIFM1)
ENST00000676229.1:c.770-42C>G (AIFM1)	ENSP00000502184.1:n.770-42C>G
ENST00000676328.1:c.782-45C>G (AIFM1)	ENSP00000502068.1:n.782-45C>G
ENST00000676436.1:c.776-42C>G (AIFM1)	ENSP00000502669.1:n.776-42C>G
ENST00000287295.7:c.782-42C>G (AIFM1)	ENSP00000287295.3:n.782-42C>G
ENST00000319908.7:c.770-42C>G (AIFM1)	ENSP00000315122.3:n.770-42C>G
ENST00000346424.6:c.107-2728C>G (AIFM1)	ENSP00000316320.3:n.107-2728C>G
ENST00000416073.6:c.782-42C>G (AIFM1)	ENSP00000402535.2:n.782-42C>G
ENST00000527892.5:c.*507-42C>G (AIFM1)	ENSP00000435955.1:n.*507-42C>G
ENST00000533719.1:n.485-42C>G (AIFM1)
ENST00000535724.5:c.782-42C>G (AIFM1)	ENSP00000446113.2:n.782-42C>G
NM_001130847.3:c.782-42C>G (AIFM1)	NP_001124319.1:n.782-42C>G
NM_004208.3:c.782-42C>G (AIFM1)	NP_004199.1:n.782-42C>G
NM_145812.2:c.770-42C>G (AIFM1)	NP_665811.1:n.770-42C>G
NM_145813.2:c.107-2728C>G (AIFM1)	NP_665812.1:n.107-2728C>G
NR_132647.1:n.870-42C>G (AIFM1)
XM_017029963.2:c.30+22528G>C (RAB33A)	XP_016885452.1:n.30+22528G>C
NM_004208.4:c.782-42C>G (AIFM1) MANE Select	NP_004199.1:n.782-42C>G
NM_001130847.4:c.782-42C>G (AIFM1)	NP_001124319.1:n.782-42C>G
NM_145812.3:c.770-42C>G (AIFM1)	NP_665811.1:n.770-42C>G
NR_132647.2:n.824-42C>G (AIFM1)