Canonical Allele Identifier: CA1727583628

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96193024A= , CM000669.2:g.96193024A=	GRCh38
NC_000007.13:g.95822336A= , CM000669.1:g.95822336A=	GRCh37
NC_000007.12:g.95660272A=	NCBI36
NG_012247.1:g.134124T=
NG_012247.2:g.134124T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.615+13T= MANE Select	ENSP00000265631.6:n.615+13T=
ENST00000265631.9:c.615+13T=	ENSP00000265631.5:n.615+13T=
ENST00000416240.6:c.615+13T=	ENSP00000400101.2:n.615+13T=
NM_001160210.1:c.615+13T=	NP_001153682.1:n.615+13T=
NM_014251.2:c.615+13T=	NP_055066.1:n.615+13T=
NR_027662.1:n.690+13T=
XM_006715831.2:c.648+13T=	XP_006715894.1:n.648+13T=
XM_011515727.1:c.648+13T=	XP_011514029.1:n.648+13T=
XM_006715831.4:c.648+13T=	XP_006715894.1:n.648+13T=
XM_011515727.3:c.648+13T=	XP_011514029.1:n.648+13T=
XM_017011663.1:c.606+13T=	XP_016867152.1:n.606+13T=
XM_017011664.2:c.-144+13T=	XP_016867153.1:n.-144+13T=
XM_017011665.1:c.-144+13T=	XP_016867154.1:n.-144+13T=
XR_001744525.2:n.786+13T=
XR_002956405.1:n.928+13T=
NM_014251.3:c.615+13T= MANE Select	NP_055066.1:n.615+13T=
NR_027662.2:n.641+13T=
NM_001160210.2:c.615+13T=	NP_001153682.1:n.615+13T=