Canonical Allele Identifier: CA1727518616

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96122010C= , CM000669.2:g.96122010C=	GRCh38
NC_000007.13:g.95751322C= , CM000669.1:g.95751322C=	GRCh37
NC_000007.12:g.95589258C=	NCBI36
NG_012247.1:g.205138G=
NG_012247.2:g.205138G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1592-13G= MANE Select	ENSP00000265631.6:n.1592-13G=
ENST00000265631.9:c.1592-13G=	ENSP00000265631.5:n.1592-13G=
ENST00000416240.6:c.1595-13G=	ENSP00000400101.2:n.1595-13G=
NM_001160210.1:c.1595-13G=	NP_001153682.1:n.1595-13G=
NM_014251.2:c.1592-13G=	NP_055066.1:n.1592-13G=
NR_027662.1:n.1667-13G=
XM_006715831.2:c.1625-13G=	XP_006715894.1:n.1625-13G=
XM_011515728.1:c.740-13G=	XP_011514030.1:n.740-13G=
XM_006715831.4:c.1625-13G=	XP_006715894.1:n.1625-13G=
XM_017011663.1:c.1583-13G=	XP_016867152.1:n.1583-13G=
XM_017011664.2:c.740-13G=	XP_016867153.1:n.740-13G=
XM_017011665.1:c.740-13G=	XP_016867154.1:n.740-13G=
XR_001744525.2:n.1838-13G=
XR_002956405.1:n.2396-13G=
NM_014251.3:c.1592-13G= MANE Select	NP_055066.1:n.1592-13G=
NR_027662.2:n.1618-13G=
NM_001160210.2:c.1595-13G=	NP_001153682.1:n.1595-13G=