Canonical Allele Identifier: CA387918442
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.41381549A>C (hg19) chr13:g.40807413A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40807413A>C , CM000675.2:g.40807413A>C GRCh38
NC_000013.10:g.41381549A>C , CM000675.1:g.41381549A>C GRCh37
NC_000013.9:g.40279549A>C NCBI36
NG_012248.1:g.23003A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707033.1:c.572A>C (SLC25A15) ENSP00000516711.1:p.Tyr191Ser
ENST00000338625.9:c.572A>C (SLC25A15) MANE Select ENSP00000342267.4:p.Tyr191Ser
ENST00000338625.8:c.572A>C (SLC25A15) ENSP00000342267.4:p.Tyr191Ser
ENST00000470509.1:c.*255A>C (SLC25A15) ENSP00000431429.1:n.*255A>C
ENST00000478827.1:n.1059A>C (SLC25A15)
NM_014252.3:c.572A>C (SLC25A15) NP_055067.1:p.Tyr191Ser
NR_038258.1:n.623-6689T>G (TPTE2P5)
NR_038259.1:n.452-6689T>G (TPTE2P5)
NM_014252.4:c.572A>C (SLC25A15) MANE Select NP_055067.1:p.Tyr191Ser
Search 100 bp 5'
Search 100 bp 3'