Canonical Allele Identifier: CA363326148

Gene: AIF1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.161A>C MANE Select	ENSP00000365227.3:p.Tyr54Ser
ENST00000337917.11:c.203A>C	ENSP00000338776.7:p.Tyr68Ser
ENST00000376049.4:c.-2A>C	ENSP00000365217.4:n.-2A>C
ENST00000376059.7:c.161A>C	ENSP00000365227.3:p.Tyr54Ser
ENST00000466820.1:n.578A>C
ENST00000497362.5:n.580A>C
NM_001623.3:c.161A>C	NP_001614.3:p.Tyr54Ser
NM_004847.3:c.-2A>C	NP_004838.1:n.-2A>C
NM_032955.1:c.-2A>C	NP_116573.1:n.-2A>C
XM_005248870.3:c.161A>C	XP_005248927.1:p.Tyr54Ser
XM_005248871.1:c.224A>C	XP_005248928.1:p.Tyr75Ser
NM_001318970.1:c.-2A>C	NP_001305899.1:n.-2A>C
NM_001623.4:c.161A>C	NP_001614.3:p.Tyr54Ser
NM_032955.2:c.-2A>C	NP_116573.1:n.-2A>C
XM_005248870.4:c.161A>C	XP_005248927.1:p.Tyr54Ser
XM_017010332.1:c.-2A>C	XP_016865821.1:n.-2A>C
NM_001623.5:c.161A>C MANE Select	NP_001614.3:p.Tyr54Ser
NM_001318970.2:c.-2A>C	NP_001305899.1:n.-2A>C
NM_032955.3:c.-2A>C	NP_116573.1:n.-2A>C