Canonical Allele Identifier: CA1727583688

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96193075G= , CM000669.2:g.96193075G=	GRCh38
NC_000007.13:g.95822387G= , CM000669.1:g.95822387G=	GRCh37
NC_000007.12:g.95660323G=	NCBI36
NG_012247.1:g.134073C=
NG_012247.2:g.134073C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.577C= MANE Select	ENSP00000265631.6:p.His193=
ENST00000265631.9:c.577C=	ENSP00000265631.5:p.His193=
ENST00000416240.6:c.577C=	ENSP00000400101.2:p.His193=
NM_001160210.1:c.577C=	NP_001153682.1:p.His193=
NM_014251.2:c.577C=	NP_055066.1:p.His193=
NR_027662.1:n.652C=
XM_006715831.2:c.610C=	XP_006715894.1:p.His204=
XM_011515727.1:c.610C=	XP_011514029.1:p.His204=
XM_006715831.4:c.610C=	XP_006715894.1:p.His204=
XM_011515727.3:c.610C=	XP_011514029.1:p.His204=
XM_017011663.1:c.568C=	XP_016867152.1:p.His190=
XM_017011664.2:c.-182C=	XP_016867153.1:n.-182C=
XM_017011665.1:c.-182C=	XP_016867154.1:n.-182C=
XR_001744525.2:n.748C=
XR_002956405.1:n.890C=
NM_014251.3:c.577C= MANE Select	NP_055066.1:p.His193=
NR_027662.2:n.603C=
NM_001160210.2:c.577C=	NP_001153682.1:p.His193=