Canonical Allele Identifier: CA1727580785

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189654G= , CM000669.2:g.96189654G=	GRCh38
NC_000007.13:g.95818966G= , CM000669.1:g.95818966G=	GRCh37
NC_000007.12:g.95656902G=	NCBI36
NG_012247.1:g.137494C=
NG_012247.2:g.137494C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.775C= MANE Select	ENSP00000265631.6:p.Gln259=
ENST00000265631.9:c.775C=	ENSP00000265631.5:p.Gln259=
ENST00000416240.6:c.775C=	ENSP00000400101.2:p.Gln259=
NM_001160210.1:c.775C=	NP_001153682.1:p.Gln259=
NM_014251.2:c.775C=	NP_055066.1:p.Gln259=
NR_027662.1:n.850C=
XM_006715831.2:c.808C=	XP_006715894.1:p.Gln270=
XM_011515727.1:c.808C=	XP_011514029.1:p.Gln270=
XM_011515728.1:c.-4-276C=	XP_011514030.1:n.-4-276C=
XM_006715831.4:c.808C=	XP_006715894.1:p.Gln270=
XM_011515727.3:c.808C=	XP_011514029.1:p.Gln270=
XM_017011663.1:c.766C=	XP_016867152.1:p.Gln256=
XM_017011664.2:c.-4-276C=	XP_016867153.1:n.-4-276C=
XM_017011665.1:c.-4-276C=	XP_016867154.1:n.-4-276C=
XR_001744525.2:n.946C=
XR_002956405.1:n.1088C=
NM_014251.3:c.775C= MANE Select	NP_055066.1:p.Gln259=
NR_027662.2:n.801C=
NM_001160210.2:c.775C=	NP_001153682.1:p.Gln259=