Canonical Allele Identifier: CA1727574836

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96184126C= , CM000669.2:g.96184126C=	GRCh38
NC_000007.13:g.95813438C= , CM000669.1:g.95813438C=	GRCh37
NC_000007.12:g.95651374C=	NCBI36
NG_012247.1:g.143022G=
NG_012247.2:g.143022G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1177+151G= MANE Select	ENSP00000265631.6:n.1177+151G=
ENST00000265631.9:c.1177+151G=	ENSP00000265631.5:n.1177+151G=
ENST00000416240.6:c.1180+151G=	ENSP00000400101.2:n.1180+151G=
ENST00000484495.5:n.330+151G=
ENST00000490072.5:n.244+151G=
ENST00000492869.1:n.298+151G=
NM_001160210.1:c.1180+151G=	NP_001153682.1:n.1180+151G=
NM_014251.2:c.1177+151G=	NP_055066.1:n.1177+151G=
NR_027662.1:n.1252+151G=
XM_006715831.2:c.1210+151G=	XP_006715894.1:n.1210+151G=
XM_011515727.1:c.1210+151G=	XP_011514029.1:n.1210+151G=
XM_011515728.1:c.325+151G=	XP_011514030.1:n.325+151G=
XM_006715831.4:c.1210+151G=	XP_006715894.1:n.1210+151G=
XM_011515727.3:c.1210+151G=	XP_011514029.1:n.1210+151G=
XM_017011663.1:c.1168+151G=	XP_016867152.1:n.1168+151G=
XM_017011664.2:c.325+151G=	XP_016867153.1:n.325+151G=
XM_017011665.1:c.325+151G=	XP_016867154.1:n.325+151G=
XR_001744525.2:n.1348+151G=
XR_002956405.1:n.1981+151G=
NM_014251.3:c.1177+151G= MANE Select	NP_055066.1:n.1177+151G=
NR_027662.2:n.1203+151G=
NM_001160210.2:c.1180+151G=	NP_001153682.1:n.1180+151G=