Canonical Allele Identifier: CA360697833

Gene: SLC25A46

Linked Data

• dbSNP Id: rs1237184283
• MyVariant Identifiers: chr5:g.110097439T>G (hg19) ; chr5:g.110761739T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761739T>G , CM000667.2:g.110761739T>G	GRCh38
NC_000005.9:g.110097439T>G , CM000667.1:g.110097439T>G	GRCh37
NC_000005.8:g.110125338T>G	NCBI36
NG_051334.1:g.28604T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1214T>G MANE Select	ENSP00000348211.3:p.Ile405Ser
ENST00000355943.7:c.1214T>G	ENSP00000348211.3:p.Ile405Ser
ENST00000447245.6:c.971T>G	ENSP00000399717.2:p.Ile324Ser
ENST00000504098.1:c.776T>G	ENSP00000425708.1:p.Ile259Ser
ENST00000509432.1:c.575T>G	ENSP00000426604.1:p.Ile192Ser
ENST00000513706.2:n.2814T>G
ENST00000513807.5:c.728T>G	ENSP00000421134.1:p.Ile243Ser
NM_001303249.1:c.971T>G	NP_001290178.1:p.Ile324Ser
NM_001303250.1:c.941T>G	NP_001290179.1:p.Ile314Ser
NM_138773.2:c.1214T>G	NP_620128.1:p.Ile405Ser
NM_001303249.2:c.971T>G	NP_001290178.1:p.Ile324Ser
NM_001303250.2:c.941T>G	NP_001290179.1:p.Ile314Ser
NM_138773.3:c.1214T>G	NP_620128.1:p.Ile405Ser
NR_138151.1:n.1488T>G
NM_138773.4:c.1214T>G MANE Select	NP_620128.1:p.Ile405Ser
NM_001303249.3:c.971T>G	NP_001290178.1:p.Ile324Ser
NM_001303250.3:c.941T>G	NP_001290179.1:p.Ile314Ser
NR_138151.2:n.1453T>G