Canonical Allele Identifier: CA1727580329

Gene: SLC25A13

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.96189396A= , CM000669.2:g.96189396A=	GRCh38
NC_000007.13:g.95818708A= , CM000669.1:g.95818708A=	GRCh37
NC_000007.12:g.95656644A=	NCBI36
NG_012247.1:g.137752T=
NG_012247.2:g.137752T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265631.10:c.849-18T= MANE Select	ENSP00000265631.6:n.849-18T=
ENST00000265631.9:c.849-18T=	ENSP00000265631.5:n.849-18T=
ENST00000416240.6:c.849-18T=	ENSP00000400101.2:n.849-18T=
NM_001160210.1:c.849-18T=	NP_001153682.1:n.849-18T=
NM_014251.2:c.849-18T=	NP_055066.1:n.849-18T=
NR_027662.1:n.924-18T=
XM_006715831.2:c.882-18T=	XP_006715894.1:n.882-18T=
XM_011515727.1:c.882-18T=	XP_011514029.1:n.882-18T=
XM_011515728.1:c.-4-18T=	XP_011514030.1:n.-4-18T=
XM_006715831.4:c.882-18T=	XP_006715894.1:n.882-18T=
XM_011515727.3:c.882-18T=	XP_011514029.1:n.882-18T=
XM_017011663.1:c.840-18T=	XP_016867152.1:n.840-18T=
XM_017011664.2:c.-4-18T=	XP_016867153.1:n.-4-18T=
XM_017011665.1:c.-4-18T=	XP_016867154.1:n.-4-18T=
XR_001744525.2:n.1020-18T=
XR_002956405.1:n.1162-18T=
NM_014251.3:c.849-18T= MANE Select	NP_055066.1:n.849-18T=
NR_027662.2:n.875-18T=
NM_001160210.2:c.849-18T=	NP_001153682.1:n.849-18T=