Canonical Allele Identifier: CA248373857

Gene: SLC25A15 TPTE2P5

Linked Data

• dbSNP Id: rs987719565
• gnomAD v4: 13-40798825-T-C
• MyVariant Identifiers: chr13:g.41372961T>C (hg19) ; chr13:g.40798825T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.40798825T>C , CM000675.2:g.40798825T>C	GRCh38
NC_000013.10:g.41372961T>C , CM000675.1:g.41372961T>C	GRCh37
NC_000013.9:g.40270961T>C	NCBI36
NG_012248.1:g.14415T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707033.1:c.56-232T>C (SLC25A15)	ENSP00000516711.1:n.56-232T>C
ENST00000338625.9:c.56-232T>C (SLC25A15) MANE Select	ENSP00000342267.4:n.56-232T>C
ENST00000338625.8:c.56-232T>C (SLC25A15)	ENSP00000342267.4:n.56-232T>C
ENST00000417731.5:c.56-232T>C (SLC25A15)	ENSP00000415826.1:n.56-232T>C
ENST00000470509.1:c.56-232T>C (SLC25A15)	ENSP00000431429.1:n.56-232T>C
ENST00000478827.1:n.377-232T>C (SLC25A15)
NM_014252.3:c.56-232T>C (SLC25A15)	NP_055067.1:n.56-232T>C
NR_038258.1:n.2522A>G (TPTE2P5)
NR_038259.1:n.2351A>G (TPTE2P5)
NM_014252.4:c.56-232T>C (SLC25A15) MANE Select	NP_055067.1:n.56-232T>C