Canonical Allele Identifier: CA445803858

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110096954A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761254A>C , CM000667.2:g.110761254A>C	GRCh38
NC_000005.9:g.110096954A>C , CM000667.1:g.110096954A>C	GRCh37
NC_000005.8:g.110124853A>C	NCBI36
NG_051334.1:g.28119A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.729A>C MANE Select	ENSP00000348211.3:p.Gly243=
ENST00000355943.7:c.729A>C	ENSP00000348211.3:p.Gly243=
ENST00000447245.6:c.679-193A>C	ENSP00000399717.2:n.679-193A>C
ENST00000502462.6:n.1045A>C
ENST00000504098.1:c.291A>C	ENSP00000425708.1:p.Gly97=
ENST00000509432.1:c.90A>C	ENSP00000426604.1:p.Gly30=
ENST00000513706.2:n.2329A>C
ENST00000513807.5:c.243A>C	ENSP00000421134.1:p.Gly81=
NM_001303249.1:c.679-193A>C	NP_001290178.1:n.679-193A>C
NM_001303250.1:c.456A>C	NP_001290179.1:p.Gly152=
NM_138773.2:c.729A>C	NP_620128.1:p.Gly243=
NM_001303249.2:c.679-193A>C	NP_001290178.1:n.679-193A>C
NM_001303250.2:c.456A>C	NP_001290179.1:p.Gly152=
NM_138773.3:c.729A>C	NP_620128.1:p.Gly243=
NR_138151.1:n.1003A>C
NM_138773.4:c.729A>C MANE Select	NP_620128.1:p.Gly243=
NM_001303249.3:c.679-193A>C	NP_001290178.1:n.679-193A>C
NM_001303250.3:c.456A>C	NP_001290179.1:p.Gly152=
NR_138151.2:n.968A>C