Canonical Allele Identifier: CA445964601

Gene: SLC25A46

Linked Data

• gnomAD v4: 5-110761449-T-C
• MyVariant Identifiers: chr5:g.110097149T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761449T>C , CM000667.2:g.110761449T>C	GRCh38
NC_000005.9:g.110097149T>C , CM000667.1:g.110097149T>C	GRCh37
NC_000005.8:g.110125048T>C	NCBI36
NG_051334.1:g.28314T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355943.8:c.924T>C MANE Select	ENSP00000348211.3:p.Ser308=
ENST00000355943.7:c.924T>C	ENSP00000348211.3:p.Ser308=
ENST00000447245.6:c.681T>C	ENSP00000399717.2:p.Ser227=
ENST00000502462.6:n.1240T>C
ENST00000504098.1:c.486T>C	ENSP00000425708.1:p.Ser162=
ENST00000509432.1:c.285T>C	ENSP00000426604.1:p.Ser95=
ENST00000513706.2:n.2524T>C
ENST00000513807.5:c.438T>C	ENSP00000421134.1:p.Ser146=
NM_001303249.1:c.681T>C	NP_001290178.1:p.Ser227=
NM_001303250.1:c.651T>C	NP_001290179.1:p.Ser217=
NM_138773.2:c.924T>C	NP_620128.1:p.Ser308=
NM_001303249.2:c.681T>C	NP_001290178.1:p.Ser227=
NM_001303250.2:c.651T>C	NP_001290179.1:p.Ser217=
NM_138773.3:c.924T>C	NP_620128.1:p.Ser308=
NR_138151.1:n.1198T>C
NM_138773.4:c.924T>C MANE Select	NP_620128.1:p.Ser308=
NM_001303249.3:c.681T>C	NP_001290178.1:p.Ser227=
NM_001303250.3:c.651T>C	NP_001290179.1:p.Ser217=
NR_138151.2:n.1163T>C