Canonical Allele Identifier: CA387916850
Community Standard Title: NM_014252.4(SLC25A15):c.169C>T (p.Gln57Ter)
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40799170C>T , CM000675.2:g.40799170C>T GRCh38
NC_000013.10:g.41373306C>T , CM000675.1:g.41373306C>T GRCh37
NC_000013.9:g.40271306C>T NCBI36
NG_012248.1:g.14760C>T

Transcript Alleles

HGVS Amino-acid Change
NM_014252.4:c.169C>T (SLC25A15) MANE Select NP_055067.1:p.Gln57Ter
ENST00000338625.9:c.169C>T (SLC25A15) MANE Select ENSP00000342267.4:p.Gln57Ter
NM_014252.3:c.169C>T (SLC25A15) NP_055067.1:p.Gln57Ter
NR_038258.1:n.2177G>A (TPTE2P5)
NR_038259.1:n.2006G>A (TPTE2P5)
ENST00000338625.8:c.169C>T (SLC25A15) ENSP00000342267.4:p.Gln57Ter
ENST00000417731.5:c.169C>T (SLC25A15) ENSP00000415826.1:p.Gln57Ter
ENST00000470509.1:c.169C>T (SLC25A15) ENSP00000431429.1:p.Gln57Ter
ENST00000478827.1:n.490C>T (SLC25A15)
ENST00000707033.1:c.169C>T (SLC25A15) ENSP00000516711.1:p.Gln57Ter