Canonical Allele Identifier: CA801866397

Gene: SLC25A46

Linked Data

• dbSNP Id: rs1466046139
• gnomAD v3: 5-110761862-A-C
• gnomAD v4: 5-110761862-A-C
• MyVariant Identifiers: chr5:g.110097562A>C (hg19) ; chr5:g.110761862A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761862A>C , CM000667.2:g.110761862A>C	GRCh38
NC_000005.9:g.110097562A>C , CM000667.1:g.110097562A>C	GRCh37
NC_000005.8:g.110125461A>C	NCBI36
NG_051334.1:g.28727A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.*80A>C MANE Select	ENSP00000348211.3:n.*80A>C
ENST00000355943.7:c.*80A>C	ENSP00000348211.3:n.*80A>C
ENST00000447245.6:c.*80A>C	ENSP00000399717.2:n.*80A>C
ENST00000504098.1:c.*80A>C	ENSP00000425708.1:n.*80A>C
ENST00000509432.1:c.*80A>C	ENSP00000426604.1:n.*80A>C
ENST00000513706.2:n.2937A>C
ENST00000513807.5:c.*80A>C	ENSP00000421134.1:n.*80A>C
NM_001303249.1:c.*80A>C	NP_001290178.1:n.*80A>C
NM_001303250.1:c.*80A>C	NP_001290179.1:n.*80A>C
NM_138773.2:c.*80A>C	NP_620128.1:n.*80A>C
NM_001303249.2:c.*80A>C	NP_001290178.1:n.*80A>C
NM_001303250.2:c.*80A>C	NP_001290179.1:n.*80A>C
NM_138773.3:c.*80A>C	NP_620128.1:n.*80A>C
NR_138151.1:n.1611A>C
NM_138773.4:c.*80A>C MANE Select	NP_620128.1:n.*80A>C
NM_001303249.3:c.*80A>C	NP_001290178.1:n.*80A>C
NM_001303250.3:c.*80A>C	NP_001290179.1:n.*80A>C
NR_138151.2:n.1576A>C