Canonical Allele Identifier: CA360697906

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097459A>C (hg19) ; chr5:g.110761759A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761759A>C , CM000667.2:g.110761759A>C	GRCh38
NC_000005.9:g.110097459A>C , CM000667.1:g.110097459A>C	GRCh37
NC_000005.8:g.110125358A>C	NCBI36
NG_051334.1:g.28624A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1234A>C MANE Select	ENSP00000348211.3:p.Thr412Pro
ENST00000355943.7:c.1234A>C	ENSP00000348211.3:p.Thr412Pro
ENST00000447245.6:c.991A>C	ENSP00000399717.2:p.Thr331Pro
ENST00000504098.1:c.796A>C	ENSP00000425708.1:p.Thr266Pro
ENST00000509432.1:c.595A>C	ENSP00000426604.1:p.Thr199Pro
ENST00000513706.2:n.2834A>C
ENST00000513807.5:c.748A>C	ENSP00000421134.1:p.Thr250Pro
NM_001303249.1:c.991A>C	NP_001290178.1:p.Thr331Pro
NM_001303250.1:c.961A>C	NP_001290179.1:p.Thr321Pro
NM_138773.2:c.1234A>C	NP_620128.1:p.Thr412Pro
NM_001303249.2:c.991A>C	NP_001290178.1:p.Thr331Pro
NM_001303250.2:c.961A>C	NP_001290179.1:p.Thr321Pro
NM_138773.3:c.1234A>C	NP_620128.1:p.Thr412Pro
NR_138151.1:n.1508A>C
NM_138773.4:c.1234A>C MANE Select	NP_620128.1:p.Thr412Pro
NM_001303249.3:c.991A>C	NP_001290178.1:p.Thr331Pro
NM_001303250.3:c.961A>C	NP_001290179.1:p.Thr321Pro
NR_138151.2:n.1473A>C