Canonical Allele Identifier: CA483460788
Gene: SLC25A15 HGNC NCBI
TPTE2P5 HGNC NCBI

Linked Data

dbSNP Id: rs1882227528
MyVariant Identifiers: chr13:g.41381448C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.40807312C>T , CM000675.2:g.40807312C>T GRCh38
NC_000013.10:g.41381448C>T , CM000675.1:g.41381448C>T GRCh37
NC_000013.9:g.40279448C>T NCBI36
NG_012248.1:g.22902C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000707033.1:c.471C>T (SLC25A15) ENSP00000516711.1:p.Ile157=
ENST00000338625.9:c.471C>T (SLC25A15) MANE Select ENSP00000342267.4:p.Ile157=
ENST00000338625.8:c.471C>T (SLC25A15) ENSP00000342267.4:p.Ile157=
ENST00000417731.5:c.333C>T (SLC25A15) ENSP00000415826.1:p.Ile111=
ENST00000470509.1:c.*154C>T (SLC25A15) ENSP00000431429.1:n.*154C>T
ENST00000478827.1:n.958C>T (SLC25A15)
NM_014252.3:c.471C>T (SLC25A15) NP_055067.1:p.Ile157=
NR_038258.1:n.623-6588G>A (TPTE2P5)
NR_038259.1:n.452-6588G>A (TPTE2P5)
NM_014252.4:c.471C>T (SLC25A15) MANE Select NP_055067.1:p.Ile157=