Canonical Allele Identifier: CA609927492

Gene: SLC25A15 TPTE2P5

Linked Data

• dbSNP Id: rs1566124263
• gnomAD v2: 13-41381408-ATC-A
• gnomAD v3: 13-40807272-ATC-A
• gnomAD v4: 13-40807272-ATC-A
• MyVariant Identifiers: chr13:g.41381409_41381410del (hg19) ; chr13:g.40807273_40807274del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.40807278_40807279del , CM000675.2:g.40807278_40807279del	GRCh38
NC_000013.10:g.41381414_41381415del , CM000675.1:g.41381414_41381415del	GRCh37
NC_000013.9:g.40279414_40279415del	NCBI36
NG_012248.1:g.22868_22869del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707033.1:c.453-16_453-15del (SLC25A15)	ENSP00000516711.1:n.453-16_453-15del
ENST00000338625.9:c.453-16_453-15del (SLC25A15) MANE Select	ENSP00000342267.4:n.453-16_453-15del
ENST00000338625.8:c.453-16_453-15del (SLC25A15)	ENSP00000342267.4:n.453-16_453-15del
ENST00000417731.5:c.315-16_315-15del (SLC25A15)	ENSP00000415826.1:n.315-16_315-15del
ENST00000470509.1:c.*136-16_*136-15del (SLC25A15)	ENSP00000431429.1:n.*136-16_*136-15del
ENST00000478827.1:n.940-16_940-15del (SLC25A15)
NM_014252.3:c.453-16_453-15del (SLC25A15)	NP_055067.1:n.453-16_453-15del
NR_038258.1:n.623-6550_623-6549del (TPTE2P5)
NR_038259.1:n.452-6550_452-6549del (TPTE2P5)
NM_014252.4:c.453-16_453-15del (SLC25A15) MANE Select	NP_055067.1:n.453-16_453-15del