Canonical Allele Identifier: CA387916757

Gene: SLC25A15 TPTE2P5

Linked Data

• dbSNP Id: rs1566121276
• gnomAD v2: 13-41373261-G-C
• gnomAD v3: 13-40799125-G-C
• gnomAD v4: 13-40799125-G-C
• MyVariant Identifiers: chr13:g.41373261G>C (hg19) ; chr13:g.40799125G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.40799125G>C , CM000675.2:g.40799125G>C	GRCh38
NC_000013.10:g.41373261G>C , CM000675.1:g.41373261G>C	GRCh37
NC_000013.9:g.40271261G>C	NCBI36
NG_012248.1:g.14715G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000707033.1:c.124G>C (SLC25A15)	ENSP00000516711.1:p.Asp42His
ENST00000338625.9:c.124G>C (SLC25A15) MANE Select	ENSP00000342267.4:p.Asp42His
ENST00000338625.8:c.124G>C (SLC25A15)	ENSP00000342267.4:p.Asp42His
ENST00000417731.5:c.124G>C (SLC25A15)	ENSP00000415826.1:p.Asp42His
ENST00000470509.1:c.124G>C (SLC25A15)	ENSP00000431429.1:p.Asp42His
ENST00000478827.1:n.445G>C (SLC25A15)
NM_014252.3:c.124G>C (SLC25A15)	NP_055067.1:p.Asp42His
NR_038258.1:n.2222C>G (TPTE2P5)
NR_038259.1:n.2051C>G (TPTE2P5)
NM_014252.4:c.124G>C (SLC25A15) MANE Select	NP_055067.1:p.Asp42His