Canonical Allele Identifier: CA456509619

Gene: SLC25A13

Linked Data

• MyVariant Identifiers: chr7:g.95799363T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96170051T>A , CM000669.2:g.96170051T>A	GRCh38
NC_000007.13:g.95799363T>A , CM000669.1:g.95799363T>A	GRCh37
NC_000007.12:g.95637299T>A	NCBI36
NG_012247.1:g.157097A>T
NG_012247.2:g.157097A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1305A>T MANE Select	ENSP00000265631.6:p.Gly435=
ENST00000265631.9:c.1305A>T	ENSP00000265631.5:p.Gly435=
ENST00000416240.6:c.1308A>T	ENSP00000400101.2:p.Gly436=
ENST00000484495.5:n.458A>T
ENST00000490072.5:n.372A>T
ENST00000492869.1:n.426A>T
NM_001160210.1:c.1308A>T	NP_001153682.1:p.Gly436=
NM_014251.2:c.1305A>T	NP_055066.1:p.Gly435=
NR_027662.1:n.1380A>T
XM_006715831.2:c.1338A>T	XP_006715894.1:p.Gly446=
XM_011515727.1:c.1338A>T	XP_011514029.1:p.Gly446=
XM_011515728.1:c.453A>T	XP_011514030.1:p.Gly151=
XM_006715831.4:c.1338A>T	XP_006715894.1:p.Gly446=
XM_011515727.3:c.1338A>T	XP_011514029.1:p.Gly446=
XM_017011663.1:c.1296A>T	XP_016867152.1:p.Gly432=
XM_017011664.2:c.453A>T	XP_016867153.1:p.Gly151=
XM_017011665.1:c.453A>T	XP_016867154.1:p.Gly151=
XR_001744525.2:n.1476A>T
XR_002956405.1:n.2109A>T
NM_014251.3:c.1305A>T MANE Select	NP_055066.1:p.Gly435=
NR_027662.2:n.1331A>T
NM_001160210.2:c.1308A>T	NP_001153682.1:p.Gly436=