Canonical Allele Identifier: CA363326358

Gene: AIF1

Linked Data

• MyVariant Identifiers: chr6:g.31583905A>T (hg19) ; chr6:g.31616128A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616128A>T , CM000668.2:g.31616128A>T	GRCh38
NC_000006.11:g.31583905A>T , CM000668.1:g.31583905A>T	GRCh37
NC_000006.10:g.31691884A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.179A>T MANE Select	ENSP00000365227.3:p.Asn60Ile
ENST00000337917.11:c.221A>T	ENSP00000338776.7:p.Asn74Ile
ENST00000376049.4:c.17A>T	ENSP00000365217.4:p.Asn6Ile
ENST00000376059.7:c.179A>T	ENSP00000365227.3:p.Asn60Ile
ENST00000466820.1:n.596A>T
ENST00000497362.5:n.598A>T
NM_001623.3:c.179A>T	NP_001614.3:p.Asn60Ile
NM_004847.3:c.17A>T	NP_004838.1:p.Asn6Ile
NM_032955.1:c.17A>T	NP_116573.1:p.Asn6Ile
XM_005248870.3:c.179A>T	XP_005248927.1:p.Asn60Ile
XM_005248871.1:c.242A>T	XP_005248928.1:p.Asn81Ile
NM_001318970.1:c.17A>T	NP_001305899.1:p.Asn6Ile
NM_001623.4:c.179A>T	NP_001614.3:p.Asn60Ile
NM_032955.2:c.17A>T	NP_116573.1:p.Asn6Ile
XM_005248870.4:c.179A>T	XP_005248927.1:p.Asn60Ile
XM_017010332.1:c.17A>T	XP_016865821.1:p.Asn6Ile
NM_001623.5:c.179A>T MANE Select	NP_001614.3:p.Asn60Ile
NM_001318970.2:c.17A>T	NP_001305899.1:p.Asn6Ile
NM_032955.3:c.17A>T	NP_116573.1:p.Asn6Ile