Canonical Allele Identifier: CA387916742
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000707033.1:c.118T>G (SLC25A15) ENSP00000516711.1:p.Phe40Val
ENST00000338625.9:c.118T>G (SLC25A15) MANE Select ENSP00000342267.4:p.Phe40Val
ENST00000338625.8:c.118T>G (SLC25A15) ENSP00000342267.4:p.Phe40Val
ENST00000417731.5:c.118T>G (SLC25A15) ENSP00000415826.1:p.Phe40Val
ENST00000470509.1:c.118T>G (SLC25A15) ENSP00000431429.1:p.Phe40Val
ENST00000478827.1:n.439T>G (SLC25A15)
NM_014252.3:c.118T>G (SLC25A15) NP_055067.1:p.Phe40Val
NR_038258.1:n.2228A>C (TPTE2P5)
NR_038259.1:n.2057A>C (TPTE2P5)
NM_014252.4:c.118T>G (SLC25A15) MANE Select NP_055067.1:p.Phe40Val