Canonical Allele Identifier: CA360697882

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097451T>A (hg19) ; chr5:g.110761751T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761751T>A , CM000667.2:g.110761751T>A	GRCh38
NC_000005.9:g.110097451T>A , CM000667.1:g.110097451T>A	GRCh37
NC_000005.8:g.110125350T>A	NCBI36
NG_051334.1:g.28616T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1226T>A MANE Select	ENSP00000348211.3:p.Ile409Asn
ENST00000355943.7:c.1226T>A	ENSP00000348211.3:p.Ile409Asn
ENST00000447245.6:c.983T>A	ENSP00000399717.2:p.Ile328Asn
ENST00000504098.1:c.788T>A	ENSP00000425708.1:p.Ile263Asn
ENST00000509432.1:c.587T>A	ENSP00000426604.1:p.Ile196Asn
ENST00000513706.2:n.2826T>A
ENST00000513807.5:c.740T>A	ENSP00000421134.1:p.Ile247Asn
NM_001303249.1:c.983T>A	NP_001290178.1:p.Ile328Asn
NM_001303250.1:c.953T>A	NP_001290179.1:p.Ile318Asn
NM_138773.2:c.1226T>A	NP_620128.1:p.Ile409Asn
NM_001303249.2:c.983T>A	NP_001290178.1:p.Ile328Asn
NM_001303250.2:c.953T>A	NP_001290179.1:p.Ile318Asn
NM_138773.3:c.1226T>A	NP_620128.1:p.Ile409Asn
NR_138151.1:n.1500T>A
NM_138773.4:c.1226T>A MANE Select	NP_620128.1:p.Ile409Asn
NM_001303249.3:c.983T>A	NP_001290178.1:p.Ile328Asn
NM_001303250.3:c.953T>A	NP_001290179.1:p.Ile318Asn
NR_138151.2:n.1465T>A