Canonical Allele Identifier: CA6959828
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Linked Data

dbSNP Id: rs758783089
ExAC: 13:41383658 G / C
gnomAD v2: 13-41383658-G-C
gnomAD v4: 13-40809522-G-C
MyVariant Identifiers: chr13:g.41383658G>C (hg19) chr13:g.40809522G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40809522G>C , CM000675.2:g.40809522G>C GRCh38
NC_000013.10:g.41383658G>C , CM000675.1:g.41383658G>C GRCh37
NC_000013.9:g.40281658G>C NCBI36
NG_012248.1:g.25112G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707033.1:c.782-21G>C (SLC25A15) ENSP00000516711.1:n.782-21G>C
ENST00000338625.9:c.782-21G>C (SLC25A15) MANE Select ENSP00000342267.4:n.782-21G>C
ENST00000338625.8:c.782-21G>C (SLC25A15) ENSP00000342267.4:n.782-21G>C
NM_014252.3:c.782-21G>C (SLC25A15) NP_055067.1:n.782-21G>C
NR_038258.1:n.623-8798C>G (TPTE2P5)
NR_038259.1:n.452-8798C>G (TPTE2P5)
NM_014252.4:c.782-21G>C (SLC25A15) MANE Select NP_055067.1:n.782-21G>C
Search 100 bp 5'
Search 100 bp 3'