Canonical Allele Identifier: CA462169907

Gene: SLC25A32

Linked Data

• MyVariant Identifiers: chr8:g.104415422A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.103403194A>G , CM000670.2:g.103403194A>G	GRCh38
NC_000008.10:g.104415422A>G , CM000670.1:g.104415422A>G	GRCh37
NC_000008.9:g.104484598A>G	NCBI36
NG_047200.1:g.17142T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000707124.1:c.591T>C	ENSP00000516752.1:p.Tyr197=
ENST00000297578.9:c.522T>C MANE Select	ENSP00000297578.4:p.Tyr174=
ENST00000649416.1:c.369T>C	ENSP00000496817.1:p.Tyr123=
ENST00000297578.8:c.522T>C	ENSP00000297578.4:p.Tyr174=
ENST00000521645.5:c.392-1140T>C	ENSP00000430989.1:n.392-1140T>C
ENST00000523256.6:c.306-1140T>C	ENSP00000427737.1:n.306-1140T>C
ENST00000523866.1:c.*64T>C	ENSP00000430371.1:n.*64T>C
NM_030780.4:c.522T>C	NP_110407.2:p.Tyr174=
NR_102337.1:n.834T>C
NR_102338.1:n.1029T>C
NM_030780.5:c.522T>C MANE Select	NP_110407.2:p.Tyr174=
NR_102337.2:n.606T>C
NR_102338.2:n.801T>C