Canonical Allele Identifier: CA387916699
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40799100G>C , CM000675.2:g.40799100G>C GRCh38
NC_000013.10:g.41373236G>C , CM000675.1:g.41373236G>C GRCh37
NC_000013.9:g.40271236G>C NCBI36
NG_012248.1:g.14690G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000707033.1:c.99G>C (SLC25A15) ENSP00000516711.1:p.Met33Ile
ENST00000338625.9:c.99G>C (SLC25A15) MANE Select ENSP00000342267.4:p.Met33Ile
ENST00000338625.8:c.99G>C (SLC25A15) ENSP00000342267.4:p.Met33Ile
ENST00000417731.5:c.99G>C (SLC25A15) ENSP00000415826.1:p.Met33Ile
ENST00000470509.1:c.99G>C (SLC25A15) ENSP00000431429.1:p.Met33Ile
ENST00000478827.1:n.420G>C (SLC25A15)
NM_014252.3:c.99G>C (SLC25A15) NP_055067.1:p.Met33Ile
NR_038258.1:n.2247C>G (TPTE2P5)
NR_038259.1:n.2076C>G (TPTE2P5)
NM_014252.4:c.99G>C (SLC25A15) MANE Select NP_055067.1:p.Met33Ile