Canonical Allele Identifier: CA456510224

Gene: SLC25A13

Linked Data

• gnomAD v4: 7-96184281-A-G
• MyVariant Identifiers: chr7:g.95813593A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184281A>G , CM000669.2:g.96184281A>G	GRCh38
NC_000007.13:g.95813593A>G , CM000669.1:g.95813593A>G	GRCh37
NC_000007.12:g.95651529A>G	NCBI36
NG_012247.1:g.142867T>C
NG_012247.2:g.142867T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1173T>C MANE Select	ENSP00000265631.6:p.Tyr391=
ENST00000265631.9:c.1173T>C	ENSP00000265631.5:p.Tyr391=
ENST00000416240.6:c.1176T>C	ENSP00000400101.2:p.Tyr392=
ENST00000484495.5:n.326T>C
ENST00000490072.5:n.240T>C
ENST00000492869.1:n.294T>C
NM_001160210.1:c.1176T>C	NP_001153682.1:p.Tyr392=
NM_014251.2:c.1173T>C	NP_055066.1:p.Tyr391=
NR_027662.1:n.1248T>C
XM_006715831.2:c.1206T>C	XP_006715894.1:p.Tyr402=
XM_011515727.1:c.1206T>C	XP_011514029.1:p.Tyr402=
XM_011515728.1:c.321T>C	XP_011514030.1:p.Tyr107=
XM_006715831.4:c.1206T>C	XP_006715894.1:p.Tyr402=
XM_011515727.3:c.1206T>C	XP_011514029.1:p.Tyr402=
XM_017011663.1:c.1164T>C	XP_016867152.1:p.Tyr388=
XM_017011664.2:c.321T>C	XP_016867153.1:p.Tyr107=
XM_017011665.1:c.321T>C	XP_016867154.1:p.Tyr107=
XR_001744525.2:n.1344T>C
XR_002956405.1:n.1977T>C
NM_014251.3:c.1173T>C MANE Select	NP_055066.1:p.Tyr391=
NR_027662.2:n.1199T>C
NM_001160210.2:c.1176T>C	NP_001153682.1:p.Tyr392=