Canonical Allele Identifier: CA1727518608

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96122005A= , CM000669.2:g.96122005A=	GRCh38
NC_000007.13:g.95751317A= , CM000669.1:g.95751317A=	GRCh37
NC_000007.12:g.95589253A=	NCBI36
NG_012247.1:g.205143T=
NG_012247.2:g.205143T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1592-8T= MANE Select	ENSP00000265631.6:n.1592-8T=
ENST00000265631.9:c.1592-8T=	ENSP00000265631.5:n.1592-8T=
ENST00000416240.6:c.1595-8T=	ENSP00000400101.2:n.1595-8T=
NM_001160210.1:c.1595-8T=	NP_001153682.1:n.1595-8T=
NM_014251.2:c.1592-8T=	NP_055066.1:n.1592-8T=
NR_027662.1:n.1667-8T=
XM_006715831.2:c.1625-8T=	XP_006715894.1:n.1625-8T=
XM_011515728.1:c.740-8T=	XP_011514030.1:n.740-8T=
XM_006715831.4:c.1625-8T=	XP_006715894.1:n.1625-8T=
XM_017011663.1:c.1583-8T=	XP_016867152.1:n.1583-8T=
XM_017011664.2:c.740-8T=	XP_016867153.1:n.740-8T=
XM_017011665.1:c.740-8T=	XP_016867154.1:n.740-8T=
XR_001744525.2:n.1838-8T=
XR_002956405.1:n.2396-8T=
NM_014251.3:c.1592-8T= MANE Select	NP_055066.1:n.1592-8T=
NR_027662.2:n.1618-8T=
NM_001160210.2:c.1595-8T=	NP_001153682.1:n.1595-8T=