Canonical Allele Identifier: CA1807210299

Gene: SLC25A32

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.103403191C= , CM000670.2:g.103403191C=	GRCh38
NC_000008.10:g.104415419C= , CM000670.1:g.104415419C=	GRCh37
NC_000008.9:g.104484595C=	NCBI36
NG_047200.1:g.17145G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000707124.1:c.594G=	ENSP00000516752.1:p.Lys198=
ENST00000297578.9:c.525G= MANE Select	ENSP00000297578.4:p.Lys175=
ENST00000649416.1:c.372G=	ENSP00000496817.1:p.Lys124=
ENST00000297578.8:c.525G=	ENSP00000297578.4:p.Lys175=
ENST00000521645.5:c.392-1137G=	ENSP00000430989.1:n.392-1137G=
ENST00000523256.6:c.306-1137G=	ENSP00000427737.1:n.306-1137G=
ENST00000523866.1:c.*67G=	ENSP00000430371.1:n.*67G=
NM_030780.4:c.525G=	NP_110407.2:p.Lys175=
NR_102337.1:n.837G=
NR_102338.1:n.1032G=
NM_030780.5:c.525G= MANE Select	NP_110407.2:p.Lys175=
NR_102337.2:n.609G=
NR_102338.2:n.804G=