Canonical Allele Identifier: CA2086588756
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40798967G= , CM000675.2:g.40798967G= GRCh38
NC_000013.10:g.41373103G= , CM000675.1:g.41373103G= GRCh37
NC_000013.9:g.40271103G= NCBI36
NG_012248.1:g.14557G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000707033.1:c.56-90G= (SLC25A15) ENSP00000516711.1:n.56-90G=
ENST00000338625.9:c.56-90G= (SLC25A15) MANE Select ENSP00000342267.4:n.56-90G=
ENST00000338625.8:c.56-90G= (SLC25A15) ENSP00000342267.4:n.56-90G=
ENST00000417731.5:c.56-90G= (SLC25A15) ENSP00000415826.1:n.56-90G=
ENST00000470509.1:c.56-90G= (SLC25A15) ENSP00000431429.1:n.56-90G=
ENST00000478827.1:n.377-90G= (SLC25A15)
NM_014252.3:c.56-90G= (SLC25A15) NP_055067.1:n.56-90G=
NR_038258.1:n.2380C= (TPTE2P5)
NR_038259.1:n.2209C= (TPTE2P5)
NM_014252.4:c.56-90G= (SLC25A15) MANE Select NP_055067.1:n.56-90G=
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