Canonical Allele Identifier: CA2086592377
Community Standard Title: NM_014252.4(SLC25A15):c.535C= (p.Arg179=)
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40807376C= , CM000675.2:g.40807376C= GRCh38
NC_000013.10:g.41381512C= , CM000675.1:g.41381512C= GRCh37
NC_000013.9:g.40279512C= NCBI36
NG_012248.1:g.22966C=

Transcript Alleles

HGVS Amino-acid Change
NM_014252.4:c.535C= (SLC25A15) MANE Select NP_055067.1:p.Arg179=
ENST00000338625.9:c.535C= (SLC25A15) MANE Select ENSP00000342267.4:p.Arg179=
NM_014252.3:c.535C= (SLC25A15) NP_055067.1:p.Arg179=
NR_038258.1:n.623-6652G= (TPTE2P5)
NR_038259.1:n.452-6652G= (TPTE2P5)
ENST00000338625.8:c.535C= (SLC25A15) ENSP00000342267.4:p.Arg179=
ENST00000417731.5:c.397C= (SLC25A15) ENSP00000415826.1:p.Arg133=
ENST00000470509.1:c.*218C= (SLC25A15) ENSP00000431429.1:n.*218C=
ENST00000478827.1:n.1022C= (SLC25A15)
ENST00000707033.1:c.535C= (SLC25A15) ENSP00000516711.1:p.Arg179=