Canonical Allele Identifier: CA363326149

Gene: AIF1

Linked Data

• MyVariant Identifiers: chr6:g.31583887A>G (hg19) ; chr6:g.31616110A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616110A>G , CM000668.2:g.31616110A>G	GRCh38
NC_000006.11:g.31583887A>G , CM000668.1:g.31583887A>G	GRCh37
NC_000006.10:g.31691866A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.161A>G MANE Select	ENSP00000365227.3:p.Tyr54Cys
ENST00000337917.11:c.203A>G	ENSP00000338776.7:p.Tyr68Cys
ENST00000376049.4:c.-2A>G	ENSP00000365217.4:n.-2A>G
ENST00000376059.7:c.161A>G	ENSP00000365227.3:p.Tyr54Cys
ENST00000466820.1:n.578A>G
ENST00000497362.5:n.580A>G
NM_001623.3:c.161A>G	NP_001614.3:p.Tyr54Cys
NM_004847.3:c.-2A>G	NP_004838.1:n.-2A>G
NM_032955.1:c.-2A>G	NP_116573.1:n.-2A>G
XM_005248870.3:c.161A>G	XP_005248927.1:p.Tyr54Cys
XM_005248871.1:c.224A>G	XP_005248928.1:p.Tyr75Cys
NM_001318970.1:c.-2A>G	NP_001305899.1:n.-2A>G
NM_001623.4:c.161A>G	NP_001614.3:p.Tyr54Cys
NM_032955.2:c.-2A>G	NP_116573.1:n.-2A>G
XM_005248870.4:c.161A>G	XP_005248927.1:p.Tyr54Cys
XM_017010332.1:c.-2A>G	XP_016865821.1:n.-2A>G
NM_001623.5:c.161A>G MANE Select	NP_001614.3:p.Tyr54Cys
NM_001318970.2:c.-2A>G	NP_001305899.1:n.-2A>G
NM_032955.3:c.-2A>G	NP_116573.1:n.-2A>G