Canonical Allele Identifier: CA387916741
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40799119T>C , CM000675.2:g.40799119T>C GRCh38
NC_000013.10:g.41373255T>C , CM000675.1:g.41373255T>C GRCh37
NC_000013.9:g.40271255T>C NCBI36
NG_012248.1:g.14709T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707033.1:c.118T>C (SLC25A15) ENSP00000516711.1:p.Phe40Leu
ENST00000338625.9:c.118T>C (SLC25A15) MANE Select ENSP00000342267.4:p.Phe40Leu
ENST00000338625.8:c.118T>C (SLC25A15) ENSP00000342267.4:p.Phe40Leu
ENST00000417731.5:c.118T>C (SLC25A15) ENSP00000415826.1:p.Phe40Leu
ENST00000470509.1:c.118T>C (SLC25A15) ENSP00000431429.1:p.Phe40Leu
ENST00000478827.1:n.439T>C (SLC25A15)
NM_014252.3:c.118T>C (SLC25A15) NP_055067.1:p.Phe40Leu
NR_038258.1:n.2228A>G (TPTE2P5)
NR_038259.1:n.2057A>G (TPTE2P5)
NM_014252.4:c.118T>C (SLC25A15) MANE Select NP_055067.1:p.Phe40Leu