Canonical Allele Identifier: CA340490
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Linked Data

ClinVar Variation Id: 5995
ClinVar RCV Id: RCV000006361
dbSNP Id: rs104894430

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40799080G>A , CM000675.2:g.40799080G>A GRCh38
NC_000013.10:g.41373216G>A , CM000675.1:g.41373216G>A GRCh37
NC_000013.9:g.40271216G>A NCBI36
NG_012248.1:g.14670G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000707033.1:c.79G>A (SLC25A15) ENSP00000516711.1:p.Gly27Arg
ENST00000338625.9:c.79G>A (SLC25A15) MANE Select ENSP00000342267.4:p.Gly27Arg
ENST00000338625.8:c.79G>A (SLC25A15) ENSP00000342267.4:p.Gly27Arg
ENST00000417731.5:c.79G>A (SLC25A15) ENSP00000415826.1:p.Gly27Arg
ENST00000470509.1:c.79G>A (SLC25A15) ENSP00000431429.1:p.Gly27Arg
ENST00000478827.1:n.400G>A (SLC25A15)
NM_014252.3:c.79G>A (SLC25A15) NP_055067.1:p.Gly27Arg
NR_038258.1:n.2267C>T (TPTE2P5)
NR_038259.1:n.2096C>T (TPTE2P5)
NM_014252.4:c.79G>A (SLC25A15) MANE Select NP_055067.1:p.Gly27Arg