Canonical Allele Identifier: CA445964741

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097263A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761563A>C , CM000667.2:g.110761563A>C	GRCh38
NC_000005.9:g.110097263A>C , CM000667.1:g.110097263A>C	GRCh37
NC_000005.8:g.110125162A>C	NCBI36
NG_051334.1:g.28428A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1038A>C MANE Select	ENSP00000348211.3:p.Thr346=
ENST00000355943.7:c.1038A>C	ENSP00000348211.3:p.Thr346=
ENST00000447245.6:c.795A>C	ENSP00000399717.2:p.Thr265=
ENST00000502462.6:n.1354A>C
ENST00000504098.1:c.600A>C	ENSP00000425708.1:p.Thr200=
ENST00000509432.1:c.399A>C	ENSP00000426604.1:p.Thr133=
ENST00000513706.2:n.2638A>C
ENST00000513807.5:c.552A>C	ENSP00000421134.1:p.Thr184=
NM_001303249.1:c.795A>C	NP_001290178.1:p.Thr265=
NM_001303250.1:c.765A>C	NP_001290179.1:p.Thr255=
NM_138773.2:c.1038A>C	NP_620128.1:p.Thr346=
NM_001303249.2:c.795A>C	NP_001290178.1:p.Thr265=
NM_001303250.2:c.765A>C	NP_001290179.1:p.Thr255=
NM_138773.3:c.1038A>C	NP_620128.1:p.Thr346=
NR_138151.1:n.1312A>C
NM_138773.4:c.1038A>C MANE Select	NP_620128.1:p.Thr346=
NM_001303249.3:c.795A>C	NP_001290178.1:p.Thr265=
NM_001303250.3:c.765A>C	NP_001290179.1:p.Thr255=
NR_138151.2:n.1277A>C