Canonical Allele Identifier: CA449661617

Gene: AIF1

Linked Data

• gnomAD v4: 6-31616135-T-C
• MyVariant Identifiers: chr6:g.31583912T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616135T>C , CM000668.2:g.31616135T>C	GRCh38
NC_000006.11:g.31583912T>C , CM000668.1:g.31583912T>C	GRCh37
NC_000006.10:g.31691891T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.186T>C MANE Select	ENSP00000365227.3:p.Asn62=
ENST00000337917.11:c.228T>C	ENSP00000338776.7:p.Asn76=
ENST00000376049.4:c.24T>C	ENSP00000365217.4:p.Asn8=
ENST00000376059.7:c.186T>C	ENSP00000365227.3:p.Asn62=
ENST00000466820.1:n.603T>C
ENST00000497362.5:n.605T>C
NM_001623.3:c.186T>C	NP_001614.3:p.Asn62=
NM_004847.3:c.24T>C	NP_004838.1:p.Asn8=
NM_032955.1:c.24T>C	NP_116573.1:p.Asn8=
XM_005248870.3:c.186T>C	XP_005248927.1:p.Asn62=
XM_005248871.1:c.249T>C	XP_005248928.1:p.Asn83=
NM_001318970.1:c.24T>C	NP_001305899.1:p.Asn8=
NM_001623.4:c.186T>C	NP_001614.3:p.Asn62=
NM_032955.2:c.24T>C	NP_116573.1:p.Asn8=
XM_005248870.4:c.186T>C	XP_005248927.1:p.Asn62=
XM_017010332.1:c.24T>C	XP_016865821.1:p.Asn8=
NM_001623.5:c.186T>C MANE Select	NP_001614.3:p.Asn62=
NM_001318970.2:c.24T>C	NP_001305899.1:p.Asn8=
NM_032955.3:c.24T>C	NP_116573.1:p.Asn8=