Canonical Allele Identifier: CA445964784

Gene: SLC25A46

Linked Data

• gnomAD v4: 5-110761629-A-G
• MyVariant Identifiers: chr5:g.110097329A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761629A>G , CM000667.2:g.110761629A>G	GRCh38
NC_000005.9:g.110097329A>G , CM000667.1:g.110097329A>G	GRCh37
NC_000005.8:g.110125228A>G	NCBI36
NG_051334.1:g.28494A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1104A>G MANE Select	ENSP00000348211.3:p.Gly368=
ENST00000355943.7:c.1104A>G	ENSP00000348211.3:p.Gly368=
ENST00000447245.6:c.861A>G	ENSP00000399717.2:p.Gly287=
ENST00000502462.6:n.1420A>G
ENST00000504098.1:c.666A>G	ENSP00000425708.1:p.Gly222=
ENST00000509432.1:c.465A>G	ENSP00000426604.1:p.Gly155=
ENST00000513706.2:n.2704A>G
ENST00000513807.5:c.618A>G	ENSP00000421134.1:p.Gly206=
NM_001303249.1:c.861A>G	NP_001290178.1:p.Gly287=
NM_001303250.1:c.831A>G	NP_001290179.1:p.Gly277=
NM_138773.2:c.1104A>G	NP_620128.1:p.Gly368=
NM_001303249.2:c.861A>G	NP_001290178.1:p.Gly287=
NM_001303250.2:c.831A>G	NP_001290179.1:p.Gly277=
NM_138773.3:c.1104A>G	NP_620128.1:p.Gly368=
NR_138151.1:n.1378A>G
NM_138773.4:c.1104A>G MANE Select	NP_620128.1:p.Gly368=
NM_001303249.3:c.861A>G	NP_001290178.1:p.Gly287=
NM_001303250.3:c.831A>G	NP_001290179.1:p.Gly277=
NR_138151.2:n.1343A>G