Canonical Allele Identifier: CA1723768401

Gene: SLC25A40

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87837562T= , CM000669.2:g.87837562T=	GRCh38
NC_000007.13:g.87466877T= , CM000669.1:g.87466877T=	GRCh37
NC_000007.12:g.87304813T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341119.10:c.824-752A= MANE Select	ENSP00000344831.5:n.824-752A=
ENST00000341119.9:c.824-752A=	ENSP00000344831.5:n.824-752A=
ENST00000429674.5:c.*641-752A=	ENSP00000405566.1:n.*641-752A=
ENST00000446236.5:c.*187-752A=	ENSP00000401473.1:n.*187-752A=
ENST00000470328.1:n.636-1201A=
ENST00000496348.5:n.110-752A=
NM_018843.3:c.824-752A=	NP_061331.2:n.824-752A=
XM_005250496.3:c.824-752A=	XP_005250553.1:n.824-752A=
XM_011516401.1:c.824-752A=	XP_011514703.1:n.824-752A=
XM_011516402.1:c.824-752A=	XP_011514704.1:n.824-752A=
XM_011516403.1:c.824-1201A=	XP_011514705.1:n.824-1201A=
XM_011516404.1:c.638-752A=	XP_011514706.1:n.638-752A=
XM_011516405.1:c.638-752A=	XP_011514707.1:n.638-752A=
XR_927490.1:n.1300-752A=
NM_018843.4:c.824-752A= MANE Select	NP_061331.2:n.824-752A=