Canonical Allele Identifier: CA360697405

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097346A>T (hg19) ; chr5:g.110761646A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761646A>T , CM000667.2:g.110761646A>T	GRCh38
NC_000005.9:g.110097346A>T , CM000667.1:g.110097346A>T	GRCh37
NC_000005.8:g.110125245A>T	NCBI36
NG_051334.1:g.28511A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1121A>T MANE Select	ENSP00000348211.3:p.Asn374Ile
ENST00000355943.7:c.1121A>T	ENSP00000348211.3:p.Asn374Ile
ENST00000447245.6:c.878A>T	ENSP00000399717.2:p.Asn293Ile
ENST00000502462.6:n.1437A>T
ENST00000504098.1:c.683A>T	ENSP00000425708.1:p.Asn228Ile
ENST00000509432.1:c.482A>T	ENSP00000426604.1:p.Asn161Ile
ENST00000513706.2:n.2721A>T
ENST00000513807.5:c.635A>T	ENSP00000421134.1:p.Asn212Ile
NM_001303249.1:c.878A>T	NP_001290178.1:p.Asn293Ile
NM_001303250.1:c.848A>T	NP_001290179.1:p.Asn283Ile
NM_138773.2:c.1121A>T	NP_620128.1:p.Asn374Ile
NM_001303249.2:c.878A>T	NP_001290178.1:p.Asn293Ile
NM_001303250.2:c.848A>T	NP_001290179.1:p.Asn283Ile
NM_138773.3:c.1121A>T	NP_620128.1:p.Asn374Ile
NR_138151.1:n.1395A>T
NM_138773.4:c.1121A>T MANE Select	NP_620128.1:p.Asn374Ile
NM_001303249.3:c.878A>T	NP_001290178.1:p.Asn293Ile
NM_001303250.3:c.848A>T	NP_001290179.1:p.Asn283Ile
NR_138151.2:n.1360A>T