Canonical Allele Identifier: CA6959636

Gene: SLC25A15 TPTE2P5

Linked Data

• dbSNP Id: rs778342930
• ExAC: 13:41373289 G / A
• gnomAD v2: 13-41373289-G-A
• gnomAD v4: 13-40799153-G-A
• MyVariant Identifiers: chr13:g.41373289G>A (hg19) ; chr13:g.40799153G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.40799153G>A , CM000675.2:g.40799153G>A	GRCh38
NC_000013.10:g.41373289G>A , CM000675.1:g.41373289G>A	GRCh37
NC_000013.9:g.40271289G>A	NCBI36
NG_012248.1:g.14743G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707033.1:c.152G>A (SLC25A15)	ENSP00000516711.1:p.Cys51Tyr
ENST00000338625.9:c.152G>A (SLC25A15) MANE Select	ENSP00000342267.4:p.Cys51Tyr
ENST00000338625.8:c.152G>A (SLC25A15)	ENSP00000342267.4:p.Cys51Tyr
ENST00000417731.5:c.152G>A (SLC25A15)	ENSP00000415826.1:p.Cys51Tyr
ENST00000470509.1:c.152G>A (SLC25A15)	ENSP00000431429.1:p.Cys51Tyr
ENST00000478827.1:n.473G>A (SLC25A15)
NM_014252.3:c.152G>A (SLC25A15)	NP_055067.1:p.Cys51Tyr
NR_038258.1:n.2194C>T (TPTE2P5)
NR_038259.1:n.2023C>T (TPTE2P5)
NM_014252.4:c.152G>A (SLC25A15) MANE Select	NP_055067.1:p.Cys51Tyr