Canonical Allele Identifier: CA387918014
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40807296C>A , CM000675.2:g.40807296C>A GRCh38
NC_000013.10:g.41381432C>A , CM000675.1:g.41381432C>A GRCh37
NC_000013.9:g.40279432C>A NCBI36
NG_012248.1:g.22886C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707033.1:c.455C>A (SLC25A15) ENSP00000516711.1:p.Thr152Lys
ENST00000338625.9:c.455C>A (SLC25A15) MANE Select ENSP00000342267.4:p.Thr152Lys
ENST00000338625.8:c.455C>A (SLC25A15) ENSP00000342267.4:p.Thr152Lys
ENST00000417731.5:c.317C>A (SLC25A15) ENSP00000415826.1:p.Thr106Lys
ENST00000470509.1:c.*138C>A (SLC25A15) ENSP00000431429.1:n.*138C>A
ENST00000478827.1:n.942C>A (SLC25A15)
NM_014252.3:c.455C>A (SLC25A15) NP_055067.1:p.Thr152Lys
NR_038258.1:n.623-6572G>T (TPTE2P5)
NR_038259.1:n.452-6572G>T (TPTE2P5)
NM_014252.4:c.455C>A (SLC25A15) MANE Select NP_055067.1:p.Thr152Lys