Canonical Allele Identifier: CA360697806

Gene: SLC25A46

Linked Data

• gnomAD v4: 5-110761733-T-C
• MyVariant Identifiers: chr5:g.110097433T>C (hg19) ; chr5:g.110761733T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761733T>C , CM000667.2:g.110761733T>C	GRCh38
NC_000005.9:g.110097433T>C , CM000667.1:g.110097433T>C	GRCh37
NC_000005.8:g.110125332T>C	NCBI36
NG_051334.1:g.28598T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1208T>C MANE Select	ENSP00000348211.3:p.Leu403Ser
ENST00000355943.7:c.1208T>C	ENSP00000348211.3:p.Leu403Ser
ENST00000447245.6:c.965T>C	ENSP00000399717.2:p.Leu322Ser
ENST00000504098.1:c.770T>C	ENSP00000425708.1:p.Leu257Ser
ENST00000509432.1:c.569T>C	ENSP00000426604.1:p.Leu190Ser
ENST00000513706.2:n.2808T>C
ENST00000513807.5:c.722T>C	ENSP00000421134.1:p.Leu241Ser
NM_001303249.1:c.965T>C	NP_001290178.1:p.Leu322Ser
NM_001303250.1:c.935T>C	NP_001290179.1:p.Leu312Ser
NM_138773.2:c.1208T>C	NP_620128.1:p.Leu403Ser
NM_001303249.2:c.965T>C	NP_001290178.1:p.Leu322Ser
NM_001303250.2:c.935T>C	NP_001290179.1:p.Leu312Ser
NM_138773.3:c.1208T>C	NP_620128.1:p.Leu403Ser
NR_138151.1:n.1482T>C
NM_138773.4:c.1208T>C MANE Select	NP_620128.1:p.Leu403Ser
NM_001303249.3:c.965T>C	NP_001290178.1:p.Leu322Ser
NM_001303250.3:c.935T>C	NP_001290179.1:p.Leu312Ser
NR_138151.2:n.1447T>C