Canonical Allele Identifier: CA801878208

Gene: SLC25A46

Linked Data

• dbSNP Id: rs1376106126
• gnomAD v3: 5-110746211-T-C
• gnomAD v4: 5-110746211-T-C
• MyVariant Identifiers: chr5:g.110081912T>C (hg19) ; chr5:g.110746211T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110746211T>C , CM000667.2:g.110746211T>C	GRCh38
NC_000005.9:g.110081912T>C , CM000667.1:g.110081912T>C	GRCh37
NC_000005.8:g.110109811T>C	NCBI36
NG_051334.1:g.13076T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355943.8:c.385-58T>C MANE Select	ENSP00000348211.3:n.385-58T>C
ENST00000355943.7:c.385-58T>C	ENSP00000348211.3:n.385-58T>C
ENST00000447245.6:c.385-58T>C	ENSP00000399717.2:n.385-58T>C
ENST00000502462.6:n.643T>C
ENST00000504098.1:c.-54-58T>C	ENSP00000425708.1:n.-54-58T>C
ENST00000508781.5:n.214-58T>C
ENST00000513807.5:c.-102-58T>C	ENSP00000421134.1:n.-102-58T>C
NM_001303249.1:c.385-58T>C	NP_001290178.1:n.385-58T>C
NM_001303250.1:c.112-58T>C	NP_001290179.1:n.112-58T>C
NM_138773.2:c.385-58T>C	NP_620128.1:n.385-58T>C
XM_011543708.1:c.385-58T>C	XP_011542010.1:n.385-58T>C
NM_001303249.2:c.385-58T>C	NP_001290178.1:n.385-58T>C
NM_001303250.2:c.112-58T>C	NP_001290179.1:n.112-58T>C
NM_138773.3:c.385-58T>C	NP_620128.1:n.385-58T>C
NR_138151.1:n.533-58T>C
NM_138773.4:c.385-58T>C MANE Select	NP_620128.1:n.385-58T>C
NM_001303249.3:c.385-58T>C	NP_001290178.1:n.385-58T>C
NM_001303250.3:c.112-58T>C	NP_001290179.1:n.112-58T>C
NR_138151.2:n.498-58T>C