Canonical Allele Identifier: CA1727517800

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121678C= , CM000669.2:g.96121678C=	GRCh38
NC_000007.13:g.95750990C= , CM000669.1:g.95750990C=	GRCh37
NC_000007.12:g.95588926C=	NCBI36
NG_012247.1:g.205470G=
NG_012247.2:g.205470G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1818G= MANE Select	ENSP00000265631.6:p.Trp606=
ENST00000265631.9:c.1818G=	ENSP00000265631.5:p.Trp606=
ENST00000416240.6:c.1821G=	ENSP00000400101.2:p.Trp607=
ENST00000494085.1:n.321G=
NM_001160210.1:c.1821G=	NP_001153682.1:p.Trp607=
NM_014251.2:c.1818G=	NP_055066.1:p.Trp606=
NR_027662.1:n.1893G=
XM_006715831.2:c.1851G=	XP_006715894.1:p.Trp617=
XM_011515728.1:c.966G=	XP_011514030.1:p.Trp322=
XM_006715831.4:c.1851G=	XP_006715894.1:p.Trp617=
XM_017011663.1:c.1809G=	XP_016867152.1:p.Trp603=
XM_017011664.2:c.966G=	XP_016867153.1:p.Trp322=
XM_017011665.1:c.966G=	XP_016867154.1:p.Trp322=
XR_001744525.2:n.2064G=
XR_002956405.1:n.2622G=
NM_014251.3:c.1818G= MANE Select	NP_055066.1:p.Trp606=
NR_027662.2:n.1844G=
NM_001160210.2:c.1821G=	NP_001153682.1:p.Trp607=