Canonical Allele Identifier: CA2674823675

Gene: SLC25A46

Linked Data

• gnomAD v4: 5-110761878-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761878T>C , CM000667.2:g.110761878T>C	GRCh38
NC_000005.9:g.110097578T>C , CM000667.1:g.110097578T>C	GRCh37
NC_000005.8:g.110125477T>C	NCBI36
NG_051334.1:g.28743T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.*96T>C MANE Select	ENSP00000348211.3:n.*96T>C
ENST00000355943.7:c.*96T>C	ENSP00000348211.3:n.*96T>C
ENST00000447245.6:c.*96T>C	ENSP00000399717.2:n.*96T>C
ENST00000504098.1:c.*96T>C	ENSP00000425708.1:n.*96T>C
ENST00000509432.1:c.*96T>C	ENSP00000426604.1:n.*96T>C
ENST00000513706.2:n.2953T>C
ENST00000513807.5:c.*96T>C	ENSP00000421134.1:n.*96T>C
NM_001303249.1:c.*96T>C	NP_001290178.1:n.*96T>C
NM_001303250.1:c.*96T>C	NP_001290179.1:n.*96T>C
NM_138773.2:c.*96T>C	NP_620128.1:n.*96T>C
NM_001303249.2:c.*96T>C	NP_001290178.1:n.*96T>C
NM_001303250.2:c.*96T>C	NP_001290179.1:n.*96T>C
NM_138773.3:c.*96T>C	NP_620128.1:n.*96T>C
NR_138151.1:n.1627T>C
NM_138773.4:c.*96T>C MANE Select	NP_620128.1:n.*96T>C
NM_001303249.3:c.*96T>C	NP_001290178.1:n.*96T>C
NM_001303250.3:c.*96T>C	NP_001290179.1:n.*96T>C
NR_138151.2:n.1592T>C