Canonical Allele Identifier: CA387918441
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.41381548T>C (hg19) chr13:g.40807412T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40807412T>C , CM000675.2:g.40807412T>C GRCh38
NC_000013.10:g.41381548T>C , CM000675.1:g.41381548T>C GRCh37
NC_000013.9:g.40279548T>C NCBI36
NG_012248.1:g.23002T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707033.1:c.571T>C (SLC25A15) ENSP00000516711.1:p.Tyr191His
ENST00000338625.9:c.571T>C (SLC25A15) MANE Select ENSP00000342267.4:p.Tyr191His
ENST00000338625.8:c.571T>C (SLC25A15) ENSP00000342267.4:p.Tyr191His
ENST00000470509.1:c.*254T>C (SLC25A15) ENSP00000431429.1:n.*254T>C
ENST00000478827.1:n.1058T>C (SLC25A15)
NM_014252.3:c.571T>C (SLC25A15) NP_055067.1:p.Tyr191His
NR_038258.1:n.623-6688A>G (TPTE2P5)
NR_038259.1:n.452-6688A>G (TPTE2P5)
NM_014252.4:c.571T>C (SLC25A15) MANE Select NP_055067.1:p.Tyr191His
Search 100 bp 5'
Search 100 bp 3'