Canonical Allele Identifier: CA2086592292
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40807212C= , CM000675.2:g.40807212C= GRCh38
NC_000013.10:g.41381348C= , CM000675.1:g.41381348C= GRCh37
NC_000013.9:g.40279348C= NCBI36
NG_012248.1:g.22802C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000707033.1:c.453-82C= (SLC25A15) ENSP00000516711.1:n.453-82C=
ENST00000338625.9:c.453-82C= (SLC25A15) MANE Select ENSP00000342267.4:n.453-82C=
ENST00000338625.8:c.453-82C= (SLC25A15) ENSP00000342267.4:n.453-82C=
ENST00000417731.5:c.315-82C= (SLC25A15) ENSP00000415826.1:n.315-82C=
ENST00000470509.1:c.*136-82C= (SLC25A15) ENSP00000431429.1:n.*136-82C=
ENST00000478827.1:n.940-82C= (SLC25A15)
NM_014252.3:c.453-82C= (SLC25A15) NP_055067.1:n.453-82C=
NR_038258.1:n.623-6488G= (TPTE2P5)
NR_038259.1:n.452-6488G= (TPTE2P5)
NM_014252.4:c.453-82C= (SLC25A15) MANE Select NP_055067.1:n.453-82C=