Canonical Allele Identifier: CA823905077

Gene: AIF1

Linked Data

• dbSNP Id: rs1446876288
• MyVariant Identifiers: chr6:g.31583940T>C (hg19) ; chr6:g.31616163T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31616163T>C , CM000668.2:g.31616163T>C	GRCh38
NC_000006.11:g.31583940T>C , CM000668.1:g.31583940T>C	GRCh37
NC_000006.10:g.31691919T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376059.8:c.196+18T>C MANE Select	ENSP00000365227.3:n.196+18T>C
ENST00000337917.11:c.238+18T>C	ENSP00000338776.7:n.238+18T>C
ENST00000376049.4:c.34+18T>C	ENSP00000365217.4:n.34+18T>C
ENST00000376059.7:c.196+18T>C	ENSP00000365227.3:n.196+18T>C
ENST00000466820.1:n.631T>C
ENST00000497362.5:n.633T>C
NM_001623.3:c.196+18T>C	NP_001614.3:n.196+18T>C
NM_004847.3:c.52T>C	NP_004838.1:p.Cys18Arg
NM_032955.1:c.34+18T>C	NP_116573.1:n.34+18T>C
XM_005248870.3:c.214T>C	XP_005248927.1:p.Cys72Arg
XM_005248871.1:c.259+18T>C	XP_005248928.1:n.259+18T>C
NM_001318970.1:c.34+18T>C	NP_001305899.1:n.34+18T>C
NM_001623.4:c.196+18T>C	NP_001614.3:n.196+18T>C
NM_032955.2:c.34+18T>C	NP_116573.1:n.34+18T>C
XM_005248870.4:c.214T>C	XP_005248927.1:p.Cys72Arg
XM_017010332.1:c.52T>C	XP_016865821.1:p.Cys18Arg
NM_001623.5:c.196+18T>C MANE Select	NP_001614.3:n.196+18T>C
NM_001318970.2:c.34+18T>C	NP_001305899.1:n.34+18T>C
NM_032955.3:c.34+18T>C	NP_116573.1:n.34+18T>C