Canonical Allele Identifier: CA84983504

Gene: SLC25A36

Linked Data

• dbSNP Id: rs919687247
• gnomAD v3: 3-140963259-AC-A
• gnomAD v4: 3-140963259-AC-A
• MyVariant Identifiers: chr3:g.140682102del (hg19) ; chr3:g.140963260del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.140963260del , CM000665.2:g.140963260del	GRCh38
NC_000003.11:g.140682102del , CM000665.1:g.140682102del	GRCh37
NC_000003.10:g.142164792del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324194.12:c.385+33del MANE Select	ENSP00000320688.6:n.385+33del
ENST00000648615.1:c.385+33del	ENSP00000497436.1:n.385+33del
ENST00000324194.10:c.385+33del	ENSP00000320688.6:n.385+33del
ENST00000393015.8:n.587+33del
ENST00000446041.6:c.385+33del	ENSP00000401938.2:n.385+33del
ENST00000453248.6:c.307+33del	ENSP00000391521.2:n.307+33del
ENST00000502594.5:c.385+33del	ENSP00000423319.1:n.385+33del
ENST00000507429.5:c.*19del	ENSP00000421470.1:n.*19del
ENST00000512023.5:c.235+33del	ENSP00000424505.1:n.235+33del
ENST00000512506.5:c.235+33del	ENSP00000423711.1:n.235+33del
ENST00000513887.5:c.157+33del	ENSP00000422265.1:n.157+33del
ENST00000515813.1:n.527del
ENST00000631654.1:c.385+33del	ENSP00000487839.1:n.385+33del
NM_001104647.1:c.385+33del	NP_001098117.1:n.385+33del
NM_018155.2:c.385+33del	NP_060625.2:n.385+33del
XM_006713685.2:c.-722+33del	XP_006713748.1:n.-722+33del
XM_011512951.1:c.481+33del	XP_011511253.1:n.481+33del
XM_011512952.1:c.-70+33del	XP_011511254.1:n.-70+33del
XM_011512953.1:c.481+33del	XP_011511255.1:n.481+33del
XR_924150.1:n.674+33del
XR_924151.1:n.674+33del
XR_924152.1:n.674+33del
XR_924153.1:n.674+33del
XR_924154.1:n.674+33del
XR_924155.1:n.674+33del
XR_924156.1:n.674+33del
XR_924157.1:n.674+33del
NM_001104647.3:c.385+33del MANE Select	NP_001098117.1:n.385+33del
NM_018155.3:c.385+33del	NP_060625.2:n.385+33del