Canonical Allele Identifier: CA2683824961

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96184129-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184129C>A , CM000669.2:g.96184129C>A	GRCh38
NC_000007.13:g.95813441C>A , CM000669.1:g.95813441C>A	GRCh37
NC_000007.12:g.95651377C>A	NCBI36
NG_012247.1:g.143019G>T
NG_012247.2:g.143019G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1177+148G>T MANE Select	ENSP00000265631.6:n.1177+148G>T
ENST00000265631.9:c.1177+148G>T	ENSP00000265631.5:n.1177+148G>T
ENST00000416240.6:c.1180+148G>T	ENSP00000400101.2:n.1180+148G>T
ENST00000484495.5:n.330+148G>T
ENST00000490072.5:n.244+148G>T
ENST00000492869.1:n.298+148G>T
NM_001160210.1:c.1180+148G>T	NP_001153682.1:n.1180+148G>T
NM_014251.2:c.1177+148G>T	NP_055066.1:n.1177+148G>T
NR_027662.1:n.1252+148G>T
XM_006715831.2:c.1210+148G>T	XP_006715894.1:n.1210+148G>T
XM_011515727.1:c.1210+148G>T	XP_011514029.1:n.1210+148G>T
XM_011515728.1:c.325+148G>T	XP_011514030.1:n.325+148G>T
XM_006715831.4:c.1210+148G>T	XP_006715894.1:n.1210+148G>T
XM_011515727.3:c.1210+148G>T	XP_011514029.1:n.1210+148G>T
XM_017011663.1:c.1168+148G>T	XP_016867152.1:n.1168+148G>T
XM_017011664.2:c.325+148G>T	XP_016867153.1:n.325+148G>T
XM_017011665.1:c.325+148G>T	XP_016867154.1:n.325+148G>T
XR_001744525.2:n.1348+148G>T
XR_002956405.1:n.1981+148G>T
NM_014251.3:c.1177+148G>T MANE Select	NP_055066.1:n.1177+148G>T
NR_027662.2:n.1203+148G>T
NM_001160210.2:c.1180+148G>T	NP_001153682.1:n.1180+148G>T