Canonical Allele Identifier: CA2545932472

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96184132-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184132G>A , CM000669.2:g.96184132G>A	GRCh38
NC_000007.13:g.95813444G>A , CM000669.1:g.95813444G>A	GRCh37
NC_000007.12:g.95651380G>A	NCBI36
NG_012247.1:g.143016C>T
NG_012247.2:g.143016C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1177+145C>T MANE Select	ENSP00000265631.6:n.1177+145C>T
ENST00000265631.9:c.1177+145C>T	ENSP00000265631.5:n.1177+145C>T
ENST00000416240.6:c.1180+145C>T	ENSP00000400101.2:n.1180+145C>T
ENST00000484495.5:n.330+145C>T
ENST00000490072.5:n.244+145C>T
ENST00000492869.1:n.298+145C>T
NM_001160210.1:c.1180+145C>T	NP_001153682.1:n.1180+145C>T
NM_014251.2:c.1177+145C>T	NP_055066.1:n.1177+145C>T
NR_027662.1:n.1252+145C>T
XM_006715831.2:c.1210+145C>T	XP_006715894.1:n.1210+145C>T
XM_011515727.1:c.1210+145C>T	XP_011514029.1:n.1210+145C>T
XM_011515728.1:c.325+145C>T	XP_011514030.1:n.325+145C>T
XM_006715831.4:c.1210+145C>T	XP_006715894.1:n.1210+145C>T
XM_011515727.3:c.1210+145C>T	XP_011514029.1:n.1210+145C>T
XM_017011663.1:c.1168+145C>T	XP_016867152.1:n.1168+145C>T
XM_017011664.2:c.325+145C>T	XP_016867153.1:n.325+145C>T
XM_017011665.1:c.325+145C>T	XP_016867154.1:n.325+145C>T
XR_001744525.2:n.1348+145C>T
XR_002956405.1:n.1981+145C>T
NM_014251.3:c.1177+145C>T MANE Select	NP_055066.1:n.1177+145C>T
NR_027662.2:n.1203+145C>T
NM_001160210.2:c.1180+145C>T	NP_001153682.1:n.1180+145C>T