Canonical Allele Identifier: CA955266463

Gene: SLC25A15 TPTE2P5

Linked Data

• gnomAD v3: 13-40798828-GTC-G
• gnomAD v4: 13-40798828-GTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.40798835_40798836del , CM000675.2:g.40798835_40798836del	GRCh38
NC_000013.10:g.41372971_41372972del , CM000675.1:g.41372971_41372972del	GRCh37
NC_000013.9:g.40270971_40270972del	NCBI36
NG_012248.1:g.14425_14426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707033.1:c.56-222_56-221del (SLC25A15)	ENSP00000516711.1:n.56-222_56-221del
ENST00000338625.9:c.56-222_56-221del (SLC25A15) MANE Select	ENSP00000342267.4:n.56-222_56-221del
ENST00000338625.8:c.56-222_56-221del (SLC25A15)	ENSP00000342267.4:n.56-222_56-221del
ENST00000417731.5:c.56-222_56-221del (SLC25A15)	ENSP00000415826.1:n.56-222_56-221del
ENST00000470509.1:c.56-222_56-221del (SLC25A15)	ENSP00000431429.1:n.56-222_56-221del
ENST00000478827.1:n.377-222_377-221del (SLC25A15)
NM_014252.3:c.56-222_56-221del (SLC25A15)	NP_055067.1:n.56-222_56-221del
NR_038258.1:n.2517_2518del (TPTE2P5)
NR_038259.1:n.2346_2347del (TPTE2P5)
NM_014252.4:c.56-222_56-221del (SLC25A15) MANE Select	NP_055067.1:n.56-222_56-221del