Canonical Allele Identifier: CA1572424082

Gene: SLC25A46

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761738A= , CM000667.2:g.110761738A=	GRCh38
NC_000005.9:g.110097438A= , CM000667.1:g.110097438A=	GRCh37
NC_000005.8:g.110125337A=	NCBI36
NG_051334.1:g.28603A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1213A= MANE Select	ENSP00000348211.3:p.Ile405=
ENST00000355943.7:c.1213A=	ENSP00000348211.3:p.Ile405=
ENST00000447245.6:c.970A=	ENSP00000399717.2:p.Ile324=
ENST00000504098.1:c.775A=	ENSP00000425708.1:p.Ile259=
ENST00000509432.1:c.574A=	ENSP00000426604.1:p.Ile192=
ENST00000513706.2:n.2813A=
ENST00000513807.5:c.727A=	ENSP00000421134.1:p.Ile243=
NM_001303249.1:c.970A=	NP_001290178.1:p.Ile324=
NM_001303250.1:c.940A=	NP_001290179.1:p.Ile314=
NM_138773.2:c.1213A=	NP_620128.1:p.Ile405=
NM_001303249.2:c.970A=	NP_001290178.1:p.Ile324=
NM_001303250.2:c.940A=	NP_001290179.1:p.Ile314=
NM_138773.3:c.1213A=	NP_620128.1:p.Ile405=
NR_138151.1:n.1487A=
NM_138773.4:c.1213A= MANE Select	NP_620128.1:p.Ile405=
NM_001303249.3:c.970A=	NP_001290178.1:p.Ile324=
NM_001303250.3:c.940A=	NP_001290179.1:p.Ile314=
NR_138151.2:n.1452A=