Canonical Allele Identifier: CA1727518147

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96121792A= , CM000669.2:g.96121792A=	GRCh38
NC_000007.13:g.95751104A= , CM000669.1:g.95751104A=	GRCh37
NC_000007.12:g.95589040A=	NCBI36
NG_012247.1:g.205356T=
NG_012247.2:g.205356T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.1751-47T= MANE Select	ENSP00000265631.6:n.1751-47T=
ENST00000265631.9:c.1751-47T=	ENSP00000265631.5:n.1751-47T=
ENST00000416240.6:c.1754-47T=	ENSP00000400101.2:n.1754-47T=
ENST00000494085.1:n.207T=
NM_001160210.1:c.1754-47T=	NP_001153682.1:n.1754-47T=
NM_014251.2:c.1751-47T=	NP_055066.1:n.1751-47T=
NR_027662.1:n.1826-47T=
XM_006715831.2:c.1784-47T=	XP_006715894.1:n.1784-47T=
XM_011515728.1:c.899-47T=	XP_011514030.1:n.899-47T=
XM_006715831.4:c.1784-47T=	XP_006715894.1:n.1784-47T=
XM_017011663.1:c.1742-47T=	XP_016867152.1:n.1742-47T=
XM_017011664.2:c.899-47T=	XP_016867153.1:n.899-47T=
XM_017011665.1:c.899-47T=	XP_016867154.1:n.899-47T=
XR_001744525.2:n.1997-47T=
XR_002956405.1:n.2555-47T=
NM_014251.3:c.1751-47T= MANE Select	NP_055066.1:n.1751-47T=
NR_027662.2:n.1777-47T=
NM_001160210.2:c.1754-47T=	NP_001153682.1:n.1754-47T=