Canonical Allele Identifier: CA2683825492

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96189511-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189511A>C , CM000669.2:g.96189511A>C	GRCh38
NC_000007.13:g.95818823A>C , CM000669.1:g.95818823A>C	GRCh37
NC_000007.12:g.95656759A>C	NCBI36
NG_012247.1:g.137637T>G
NG_012247.2:g.137637T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.848+70T>G MANE Select	ENSP00000265631.6:n.848+70T>G
ENST00000265631.9:c.848+70T>G	ENSP00000265631.5:n.848+70T>G
ENST00000416240.6:c.848+70T>G	ENSP00000400101.2:n.848+70T>G
NM_001160210.1:c.848+70T>G	NP_001153682.1:n.848+70T>G
NM_014251.2:c.848+70T>G	NP_055066.1:n.848+70T>G
NR_027662.1:n.923+70T>G
XM_006715831.2:c.881+70T>G	XP_006715894.1:n.881+70T>G
XM_011515727.1:c.881+70T>G	XP_011514029.1:n.881+70T>G
XM_011515728.1:c.-4-133T>G	XP_011514030.1:n.-4-133T>G
XM_006715831.4:c.881+70T>G	XP_006715894.1:n.881+70T>G
XM_011515727.3:c.881+70T>G	XP_011514029.1:n.881+70T>G
XM_017011663.1:c.839+70T>G	XP_016867152.1:n.839+70T>G
XM_017011664.2:c.-4-133T>G	XP_016867153.1:n.-4-133T>G
XM_017011665.1:c.-4-133T>G	XP_016867154.1:n.-4-133T>G
XR_001744525.2:n.1019+70T>G
XR_002956405.1:n.1161+70T>G
NM_014251.3:c.848+70T>G MANE Select	NP_055066.1:n.848+70T>G
NR_027662.2:n.874+70T>G
NM_001160210.2:c.848+70T>G	NP_001153682.1:n.848+70T>G