Canonical Allele Identifier: CA1406318492

Gene: SLC25A36

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.140963190T= , CM000665.2:g.140963190T=	GRCh38
NC_000003.11:g.140682032T= , CM000665.1:g.140682032T=	GRCh37
NC_000003.10:g.142164722T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324194.12:c.348T= MANE Select	ENSP00000320688.6:p.Asp116=
ENST00000648615.1:c.348T=	ENSP00000497436.1:p.Asp116=
ENST00000324194.10:c.348T=	ENSP00000320688.6:p.Asp116=
ENST00000393015.8:n.550T=
ENST00000446041.6:c.348T=	ENSP00000401938.2:p.Asp116=
ENST00000453248.6:c.270T=	ENSP00000391521.2:p.Asp90=
ENST00000502594.5:c.348T=	ENSP00000423319.1:p.Asp116=
ENST00000507429.5:c.348T=	ENSP00000421470.1:p.Asp116=
ENST00000512023.5:c.198T=	ENSP00000424505.1:p.Asp66=
ENST00000512506.5:c.198T=	ENSP00000423711.1:p.Asp66=
ENST00000513887.5:c.120T=	ENSP00000422265.1:p.Asp40=
ENST00000515813.1:n.457T=
ENST00000631654.1:c.348T=	ENSP00000487839.1:p.Asp116=
NM_001104647.1:c.348T=	NP_001098117.1:p.Asp116=
NM_018155.2:c.348T=	NP_060625.2:p.Asp116=
XM_006713685.2:c.-759T=	XP_006713748.1:n.-759T=
XM_011512951.1:c.444T=	XP_011511253.1:p.Asp148=
XM_011512952.1:c.-107T=	XP_011511254.1:n.-107T=
XM_011512953.1:c.444T=	XP_011511255.1:p.Asp148=
XR_924150.1:n.637T=
XR_924151.1:n.637T=
XR_924152.1:n.637T=
XR_924153.1:n.637T=
XR_924154.1:n.637T=
XR_924155.1:n.637T=
XR_924156.1:n.637T=
XR_924157.1:n.637T=
NM_001104647.3:c.348T= MANE Select	NP_001098117.1:p.Asp116=
NM_018155.3:c.348T=	NP_060625.2:p.Asp116=