Canonical Allele Identifier: CA1727575003

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184289C= , CM000669.2:g.96184289C=	GRCh38
NC_000007.13:g.95813601C= , CM000669.1:g.95813601C=	GRCh37
NC_000007.12:g.95651537C=	NCBI36
NG_012247.1:g.142859G=
NG_012247.2:g.142859G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265631.10:c.1165G= MANE Select	ENSP00000265631.6:p.Gly389=
ENST00000265631.9:c.1165G=	ENSP00000265631.5:p.Gly389=
ENST00000416240.6:c.1168G=	ENSP00000400101.2:p.Gly390=
ENST00000484495.5:n.318G=
ENST00000490072.5:n.232G=
ENST00000492869.1:n.286G=
NM_001160210.1:c.1168G=	NP_001153682.1:p.Gly390=
NM_014251.2:c.1165G=	NP_055066.1:p.Gly389=
NR_027662.1:n.1240G=
XM_006715831.2:c.1198G=	XP_006715894.1:p.Gly400=
XM_011515727.1:c.1198G=	XP_011514029.1:p.Gly400=
XM_011515728.1:c.313G=	XP_011514030.1:p.Gly105=
XM_006715831.4:c.1198G=	XP_006715894.1:p.Gly400=
XM_011515727.3:c.1198G=	XP_011514029.1:p.Gly400=
XM_017011663.1:c.1156G=	XP_016867152.1:p.Gly386=
XM_017011664.2:c.313G=	XP_016867153.1:p.Gly105=
XM_017011665.1:c.313G=	XP_016867154.1:p.Gly105=
XR_001744525.2:n.1336G=
XR_002956405.1:n.1969G=
NM_014251.3:c.1165G= MANE Select	NP_055066.1:p.Gly389=
NR_027662.2:n.1191G=
NM_001160210.2:c.1168G=	NP_001153682.1:p.Gly390=