Canonical Allele Identifier: CA546780309

Gene: SLC25A36

Linked Data

• dbSNP Id: rs1460730305
• gnomAD v2: 3-140681956-ATC-A
• gnomAD v4: 3-140963114-ATC-A
• MyVariant Identifiers: chr3:g.140681957_140681958del (hg19) ; chr3:g.140963115_140963116del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.140963118_140963119del , CM000665.2:g.140963118_140963119del	GRCh38
NC_000003.11:g.140681960_140681961del , CM000665.1:g.140681960_140681961del	GRCh37
NC_000003.10:g.142164650_142164651del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324194.12:c.285-9_285-8del MANE Select	ENSP00000320688.6:n.285-9_285-8del
ENST00000648615.1:c.285-9_285-8del	ENSP00000497436.1:n.285-9_285-8del
ENST00000324194.10:c.285-9_285-8del	ENSP00000320688.6:n.285-9_285-8del
ENST00000393015.8:n.487-9_487-8del
ENST00000446041.6:c.285-9_285-8del	ENSP00000401938.2:n.285-9_285-8del
ENST00000453248.6:c.207-9_207-8del	ENSP00000391521.2:n.207-9_207-8del
ENST00000502594.5:c.285-9_285-8del	ENSP00000423319.1:n.285-9_285-8del
ENST00000507429.5:c.285-9_285-8del	ENSP00000421470.1:n.285-9_285-8del
ENST00000512023.5:c.135-9_135-8del	ENSP00000424505.1:n.135-9_135-8del
ENST00000512506.5:c.135-9_135-8del	ENSP00000423711.1:n.135-9_135-8del
ENST00000513887.5:c.57-9_57-8del	ENSP00000422265.1:n.57-9_57-8del
ENST00000515813.1:n.394-9_394-8del
ENST00000631654.1:c.285-9_285-8del	ENSP00000487839.1:n.285-9_285-8del
NM_001104647.1:c.285-9_285-8del	NP_001098117.1:n.285-9_285-8del
NM_018155.2:c.285-9_285-8del	NP_060625.2:n.285-9_285-8del
XM_011512951.1:c.381-9_381-8del	XP_011511253.1:n.381-9_381-8del
XM_011512953.1:c.381-9_381-8del	XP_011511255.1:n.381-9_381-8del
XR_924150.1:n.574-9_574-8del
XR_924151.1:n.574-9_574-8del
XR_924152.1:n.574-9_574-8del
XR_924153.1:n.574-9_574-8del
XR_924154.1:n.574-9_574-8del
XR_924155.1:n.574-9_574-8del
XR_924156.1:n.574-9_574-8del
XR_924157.1:n.574-9_574-8del
NM_001104647.3:c.285-9_285-8del MANE Select	NP_001098117.1:n.285-9_285-8del
NM_018155.3:c.285-9_285-8del	NP_060625.2:n.285-9_285-8del