Canonical Allele Identifier: CA354858014

Gene: SLC25A36

Linked Data

• MyVariant Identifiers: chr3:g.140682012A>G (hg19) ; chr3:g.140963170A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.140963170A>G , CM000665.2:g.140963170A>G	GRCh38
NC_000003.11:g.140682012A>G , CM000665.1:g.140682012A>G	GRCh37
NC_000003.10:g.142164702A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324194.12:c.328A>G MANE Select	ENSP00000320688.6:p.Asn110Asp
ENST00000648615.1:c.328A>G	ENSP00000497436.1:p.Asn110Asp
ENST00000324194.10:c.328A>G	ENSP00000320688.6:p.Asn110Asp
ENST00000393015.8:n.530A>G
ENST00000446041.6:c.328A>G	ENSP00000401938.2:p.Asn110Asp
ENST00000453248.6:c.250A>G	ENSP00000391521.2:p.Asn84Asp
ENST00000502594.5:c.328A>G	ENSP00000423319.1:p.Asn110Asp
ENST00000507429.5:c.328A>G	ENSP00000421470.1:p.Asn110Asp
ENST00000512023.5:c.178A>G	ENSP00000424505.1:p.Asn60Asp
ENST00000512506.5:c.178A>G	ENSP00000423711.1:p.Asn60Asp
ENST00000513887.5:c.100A>G	ENSP00000422265.1:p.Asn34Asp
ENST00000515813.1:n.437A>G
ENST00000631654.1:c.328A>G	ENSP00000487839.1:p.Asn110Asp
NM_001104647.1:c.328A>G	NP_001098117.1:p.Asn110Asp
NM_018155.2:c.328A>G	NP_060625.2:p.Asn110Asp
XM_006713685.2:c.-779A>G	XP_006713748.1:n.-779A>G
XM_011512951.1:c.424A>G	XP_011511253.1:p.Asn142Asp
XM_011512952.1:c.-127A>G	XP_011511254.1:n.-127A>G
XM_011512953.1:c.424A>G	XP_011511255.1:p.Asn142Asp
XR_924150.1:n.617A>G
XR_924151.1:n.617A>G
XR_924152.1:n.617A>G
XR_924153.1:n.617A>G
XR_924154.1:n.617A>G
XR_924155.1:n.617A>G
XR_924156.1:n.617A>G
XR_924157.1:n.617A>G
NM_001104647.3:c.328A>G MANE Select	NP_001098117.1:p.Asn110Asp
NM_018155.3:c.328A>G	NP_060625.2:p.Asn110Asp