Canonical Allele Identifier: CA2086592395
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40807410G= , CM000675.2:g.40807410G= GRCh38
NC_000013.10:g.41381546G= , CM000675.1:g.41381546G= GRCh37
NC_000013.9:g.40279546G= NCBI36
NG_012248.1:g.23000G=

Transcript Alleles

HGVS Amino-acid change
ENST00000707033.1:c.569G= (SLC25A15) ENSP00000516711.1:p.Gly190=
ENST00000338625.9:c.569G= (SLC25A15) MANE Select ENSP00000342267.4:p.Gly190=
ENST00000338625.8:c.569G= (SLC25A15) ENSP00000342267.4:p.Gly190=
ENST00000470509.1:c.*252G= (SLC25A15) ENSP00000431429.1:n.*252G=
ENST00000478827.1:n.1056G= (SLC25A15)
NM_014252.3:c.569G= (SLC25A15) NP_055067.1:p.Gly190=
NR_038258.1:n.623-6686C= (TPTE2P5)
NR_038259.1:n.452-6686C= (TPTE2P5)
NM_014252.4:c.569G= (SLC25A15) MANE Select NP_055067.1:p.Gly190=