Canonical Allele Identifier: CA2683825408

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96189201-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189201A>G , CM000669.2:g.96189201A>G	GRCh38
NC_000007.13:g.95818513A>G , CM000669.1:g.95818513A>G	GRCh37
NC_000007.12:g.95656449A>G	NCBI36
NG_012247.1:g.137947T>C
NG_012247.2:g.137947T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.933+93T>C MANE Select	ENSP00000265631.6:n.933+93T>C
ENST00000265631.9:c.933+93T>C	ENSP00000265631.5:n.933+93T>C
ENST00000416240.6:c.933+93T>C	ENSP00000400101.2:n.933+93T>C
ENST00000484495.5:n.86+93T>C
NM_001160210.1:c.933+93T>C	NP_001153682.1:n.933+93T>C
NM_014251.2:c.933+93T>C	NP_055066.1:n.933+93T>C
NR_027662.1:n.1008+93T>C
XM_006715831.2:c.966+93T>C	XP_006715894.1:n.966+93T>C
XM_011515727.1:c.966+93T>C	XP_011514029.1:n.966+93T>C
XM_011515728.1:c.81+93T>C	XP_011514030.1:n.81+93T>C
XM_006715831.4:c.966+93T>C	XP_006715894.1:n.966+93T>C
XM_011515727.3:c.966+93T>C	XP_011514029.1:n.966+93T>C
XM_017011663.1:c.924+93T>C	XP_016867152.1:n.924+93T>C
XM_017011664.2:c.81+93T>C	XP_016867153.1:n.81+93T>C
XM_017011665.1:c.81+93T>C	XP_016867154.1:n.81+93T>C
XR_001744525.2:n.1104+93T>C
XR_002956405.1:n.1246+93T>C
NM_014251.3:c.933+93T>C MANE Select	NP_055066.1:n.933+93T>C
NR_027662.2:n.959+93T>C
NM_001160210.2:c.933+93T>C	NP_001153682.1:n.933+93T>C