Canonical Allele Identifier: CA483726445

Gene: SLC25A15 TPTE2P5

Linked Data

• ClinVar Variation Id: 1990042
• ClinVar RCV Id: RCV002771132
• MyVariant Identifiers: chr13:g.41373210C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.40799074C>T , CM000675.2:g.40799074C>T	GRCh38
NC_000013.10:g.41373210C>T , CM000675.1:g.41373210C>T	GRCh37
NC_000013.9:g.40271210C>T	NCBI36
NG_012248.1:g.14664C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707033.1:c.73C>T (SLC25A15)	ENSP00000516711.1:p.Leu25=
ENST00000338625.9:c.73C>T (SLC25A15) MANE Select	ENSP00000342267.4:p.Leu25=
ENST00000338625.8:c.73C>T (SLC25A15)	ENSP00000342267.4:p.Leu25=
ENST00000417731.5:c.73C>T (SLC25A15)	ENSP00000415826.1:p.Leu25=
ENST00000470509.1:c.73C>T (SLC25A15)	ENSP00000431429.1:p.Leu25=
ENST00000478827.1:n.394C>T (SLC25A15)
NM_014252.3:c.73C>T (SLC25A15)	NP_055067.1:p.Leu25=
NR_038258.1:n.2273G>A (TPTE2P5)
NR_038259.1:n.2102G>A (TPTE2P5)
NM_014252.4:c.73C>T (SLC25A15) MANE Select	NP_055067.1:p.Leu25=