Canonical Allele Identifier: CA371624926

Gene: SLC25A32

Linked Data

• MyVariant Identifiers: chr8:g.104415419C>A (hg19) ; chr8:g.103403191C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000707124.1:c.594G>T	ENSP00000516752.1:p.Lys198Asn
ENST00000297578.9:c.525G>T MANE Select	ENSP00000297578.4:p.Lys175Asn
ENST00000649416.1:c.372G>T	ENSP00000496817.1:p.Lys124Asn
ENST00000297578.8:c.525G>T	ENSP00000297578.4:p.Lys175Asn
ENST00000521645.5:c.392-1137G>T	ENSP00000430989.1:n.392-1137G>T
ENST00000523256.6:c.306-1137G>T	ENSP00000427737.1:n.306-1137G>T
ENST00000523866.1:c.*67G>T	ENSP00000430371.1:n.*67G>T
NM_030780.4:c.525G>T	NP_110407.2:p.Lys175Asn
NR_102337.1:n.837G>T
NR_102338.1:n.1032G>T
NM_030780.5:c.525G>T MANE Select	NP_110407.2:p.Lys175Asn
NR_102337.2:n.609G>T
NR_102338.2:n.804G>T