Canonical Allele Identifier: CA445803847

Gene: SLC25A46

Linked Data

• gnomAD v4: 5-110761230-C-T
• MyVariant Identifiers: chr5:g.110096930C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761230C>T , CM000667.2:g.110761230C>T	GRCh38
NC_000005.9:g.110096930C>T , CM000667.1:g.110096930C>T	GRCh37
NC_000005.8:g.110124829C>T	NCBI36
NG_051334.1:g.28095C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.705C>T MANE Select	ENSP00000348211.3:p.Gly235=
ENST00000355943.7:c.705C>T	ENSP00000348211.3:p.Gly235=
ENST00000447245.6:c.679-217C>T	ENSP00000399717.2:n.679-217C>T
ENST00000502462.6:n.1021C>T
ENST00000504098.1:c.267C>T	ENSP00000425708.1:p.Gly89=
ENST00000509432.1:c.66C>T	ENSP00000426604.1:p.Gly22=
ENST00000513706.2:n.2305C>T
ENST00000513807.5:c.219C>T	ENSP00000421134.1:p.Gly73=
NM_001303249.1:c.679-217C>T	NP_001290178.1:n.679-217C>T
NM_001303250.1:c.432C>T	NP_001290179.1:p.Gly144=
NM_138773.2:c.705C>T	NP_620128.1:p.Gly235=
NM_001303249.2:c.679-217C>T	NP_001290178.1:n.679-217C>T
NM_001303250.2:c.432C>T	NP_001290179.1:p.Gly144=
NM_138773.3:c.705C>T	NP_620128.1:p.Gly235=
NR_138151.1:n.979C>T
NM_138773.4:c.705C>T MANE Select	NP_620128.1:p.Gly235=
NM_001303249.3:c.679-217C>T	NP_001290178.1:n.679-217C>T
NM_001303250.3:c.432C>T	NP_001290179.1:p.Gly144=
NR_138151.2:n.944C>T