Canonical Allele Identifier: CA2683825446

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96189381-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189381G>A , CM000669.2:g.96189381G>A	GRCh38
NC_000007.13:g.95818693G>A , CM000669.1:g.95818693G>A	GRCh37
NC_000007.12:g.95656629G>A	NCBI36
NG_012247.1:g.137767C>T
NG_012247.2:g.137767C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.849-3C>T MANE Select	ENSP00000265631.6:n.849-3C>T
ENST00000265631.9:c.849-3C>T	ENSP00000265631.5:n.849-3C>T
ENST00000416240.6:c.849-3C>T	ENSP00000400101.2:n.849-3C>T
NM_001160210.1:c.849-3C>T	NP_001153682.1:n.849-3C>T
NM_014251.2:c.849-3C>T	NP_055066.1:n.849-3C>T
NR_027662.1:n.924-3C>T
XM_006715831.2:c.882-3C>T	XP_006715894.1:n.882-3C>T
XM_011515727.1:c.882-3C>T	XP_011514029.1:n.882-3C>T
XM_011515728.1:c.-4-3C>T	XP_011514030.1:n.-4-3C>T
XM_006715831.4:c.882-3C>T	XP_006715894.1:n.882-3C>T
XM_011515727.3:c.882-3C>T	XP_011514029.1:n.882-3C>T
XM_017011663.1:c.840-3C>T	XP_016867152.1:n.840-3C>T
XM_017011664.2:c.-4-3C>T	XP_016867153.1:n.-4-3C>T
XM_017011665.1:c.-4-3C>T	XP_016867154.1:n.-4-3C>T
XR_001744525.2:n.1020-3C>T
XR_002956405.1:n.1162-3C>T
NM_014251.3:c.849-3C>T MANE Select	NP_055066.1:n.849-3C>T
NR_027662.2:n.875-3C>T
NM_001160210.2:c.849-3C>T	NP_001153682.1:n.849-3C>T