Canonical Allele Identifier: CA436070414

Gene: SLC25A36

Linked Data

• gnomAD v4: 3-140963142-T-C
• MyVariant Identifiers: chr3:g.140681984T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.140963142T>C , CM000665.2:g.140963142T>C	GRCh38
NC_000003.11:g.140681984T>C , CM000665.1:g.140681984T>C	GRCh37
NC_000003.10:g.142164674T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324194.12:c.300T>C MANE Select	ENSP00000320688.6:p.Ala100=
ENST00000648615.1:c.300T>C	ENSP00000497436.1:p.Ala100=
ENST00000324194.10:c.300T>C	ENSP00000320688.6:p.Ala100=
ENST00000393015.8:n.502T>C
ENST00000446041.6:c.300T>C	ENSP00000401938.2:p.Ala100=
ENST00000453248.6:c.222T>C	ENSP00000391521.2:p.Ala74=
ENST00000502594.5:c.300T>C	ENSP00000423319.1:p.Ala100=
ENST00000507429.5:c.300T>C	ENSP00000421470.1:p.Ala100=
ENST00000512023.5:c.150T>C	ENSP00000424505.1:p.Ala50=
ENST00000512506.5:c.150T>C	ENSP00000423711.1:p.Ala50=
ENST00000513887.5:c.72T>C	ENSP00000422265.1:p.Ala24=
ENST00000515813.1:n.409T>C
ENST00000631654.1:c.300T>C	ENSP00000487839.1:p.Ala100=
NM_001104647.1:c.300T>C	NP_001098117.1:p.Ala100=
NM_018155.2:c.300T>C	NP_060625.2:p.Ala100=
XM_006713685.2:c.-807T>C	XP_006713748.1:n.-807T>C
XM_011512951.1:c.396T>C	XP_011511253.1:p.Ala132=
XM_011512952.1:c.-155T>C	XP_011511254.1:n.-155T>C
XM_011512953.1:c.396T>C	XP_011511255.1:p.Ala132=
XR_924150.1:n.589T>C
XR_924151.1:n.589T>C
XR_924152.1:n.589T>C
XR_924153.1:n.589T>C
XR_924154.1:n.589T>C
XR_924155.1:n.589T>C
XR_924156.1:n.589T>C
XR_924157.1:n.589T>C
NM_001104647.3:c.300T>C MANE Select	NP_001098117.1:p.Ala100=
NM_018155.3:c.300T>C	NP_060625.2:p.Ala100=