Canonical Allele Identifier: CA387918381
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40807397T>A , CM000675.2:g.40807397T>A GRCh38
NC_000013.10:g.41381533T>A , CM000675.1:g.41381533T>A GRCh37
NC_000013.9:g.40279533T>A NCBI36
NG_012248.1:g.22987T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707033.1:c.556T>A (SLC25A15) ENSP00000516711.1:p.Phe186Ile
ENST00000338625.9:c.556T>A (SLC25A15) MANE Select ENSP00000342267.4:p.Phe186Ile
ENST00000338625.8:c.556T>A (SLC25A15) ENSP00000342267.4:p.Phe186Ile
ENST00000470509.1:c.*239T>A (SLC25A15) ENSP00000431429.1:n.*239T>A
ENST00000478827.1:n.1043T>A (SLC25A15)
NM_014252.3:c.556T>A (SLC25A15) NP_055067.1:p.Phe186Ile
NR_038258.1:n.623-6673A>T (TPTE2P5)
NR_038259.1:n.452-6673A>T (TPTE2P5)
NM_014252.4:c.556T>A (SLC25A15) MANE Select NP_055067.1:p.Phe186Ile