Canonical Allele Identifier: CA387916909

Gene: SLC25A15 TPTE2P5

Linked Data

• gnomAD v4: 13-40799198-G-T
• MyVariant Identifiers: chr13:g.41373334G>T (hg19) ; chr13:g.40799198G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.40799198G>T , CM000675.2:g.40799198G>T	GRCh38
NC_000013.10:g.41373334G>T , CM000675.1:g.41373334G>T	GRCh37
NC_000013.9:g.40271334G>T	NCBI36
NG_012248.1:g.14788G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707033.1:c.197G>T (SLC25A15)	ENSP00000516711.1:p.Gly66Val
ENST00000338625.9:c.197G>T (SLC25A15) MANE Select	ENSP00000342267.4:p.Gly66Val
ENST00000338625.8:c.197G>T (SLC25A15)	ENSP00000342267.4:p.Gly66Val
ENST00000417731.5:c.197G>T (SLC25A15)	ENSP00000415826.1:p.Gly66Val
ENST00000470509.1:c.171+26G>T (SLC25A15)	ENSP00000431429.1:n.171+26G>T
ENST00000478827.1:n.518G>T (SLC25A15)
NM_014252.3:c.197G>T (SLC25A15)	NP_055067.1:p.Gly66Val
NR_038258.1:n.2149C>A (TPTE2P5)
NR_038259.1:n.1978C>A (TPTE2P5)
NM_014252.4:c.197G>T (SLC25A15) MANE Select	NP_055067.1:p.Gly66Val