Canonical Allele Identifier: CA371625005

Gene: SLC25A32

Linked Data

• MyVariant Identifiers: chr8:g.104415432A>C (hg19) ; chr8:g.103403204A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.103403204A>C , CM000670.2:g.103403204A>C	GRCh38
NC_000008.10:g.104415432A>C , CM000670.1:g.104415432A>C	GRCh37
NC_000008.9:g.104484608A>C	NCBI36
NG_047200.1:g.17132T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000707124.1:c.581T>G	ENSP00000516752.1:p.Val194Gly
ENST00000297578.9:c.512T>G MANE Select	ENSP00000297578.4:p.Val171Gly
ENST00000649416.1:c.359T>G	ENSP00000496817.1:p.Val120Gly
ENST00000297578.8:c.512T>G	ENSP00000297578.4:p.Val171Gly
ENST00000521645.5:c.392-1150T>G	ENSP00000430989.1:n.392-1150T>G
ENST00000523256.6:c.306-1150T>G	ENSP00000427737.1:n.306-1150T>G
ENST00000523866.1:c.*54T>G	ENSP00000430371.1:n.*54T>G
NM_030780.4:c.512T>G	NP_110407.2:p.Val171Gly
NR_102337.1:n.824T>G
NR_102338.1:n.1019T>G
NM_030780.5:c.512T>G MANE Select	NP_110407.2:p.Val171Gly
NR_102337.2:n.596T>G
NR_102338.2:n.791T>G