Canonical Allele Identifier: CA360697735

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097420C>G (hg19) ; chr5:g.110761720C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761720C>G , CM000667.2:g.110761720C>G	GRCh38
NC_000005.9:g.110097420C>G , CM000667.1:g.110097420C>G	GRCh37
NC_000005.8:g.110125319C>G	NCBI36
NG_051334.1:g.28585C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1195C>G MANE Select	ENSP00000348211.3:p.His399Asp
ENST00000355943.7:c.1195C>G	ENSP00000348211.3:p.His399Asp
ENST00000447245.6:c.952C>G	ENSP00000399717.2:p.His318Asp
ENST00000504098.1:c.757C>G	ENSP00000425708.1:p.His253Asp
ENST00000509432.1:c.556C>G	ENSP00000426604.1:p.His186Asp
ENST00000513706.2:n.2795C>G
ENST00000513807.5:c.709C>G	ENSP00000421134.1:p.His237Asp
NM_001303249.1:c.952C>G	NP_001290178.1:p.His318Asp
NM_001303250.1:c.922C>G	NP_001290179.1:p.His308Asp
NM_138773.2:c.1195C>G	NP_620128.1:p.His399Asp
NM_001303249.2:c.952C>G	NP_001290178.1:p.His318Asp
NM_001303250.2:c.922C>G	NP_001290179.1:p.His308Asp
NM_138773.3:c.1195C>G	NP_620128.1:p.His399Asp
NR_138151.1:n.1469C>G
NM_138773.4:c.1195C>G MANE Select	NP_620128.1:p.His399Asp
NM_001303249.3:c.952C>G	NP_001290178.1:p.His318Asp
NM_001303250.3:c.922C>G	NP_001290179.1:p.His308Asp
NR_138151.2:n.1434C>G