Canonical Allele Identifier: CA546779363

Gene: SLC25A36

Linked Data

• dbSNP Id: rs1165623977
• gnomAD v2: 3-140676725-T-C
• gnomAD v3: 3-140957883-T-C
• gnomAD v4: 3-140957883-T-C
• MyVariant Identifiers: chr3:g.140676725T>C (hg19) ; chr3:g.140957883T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.140957883T>C , CM000665.2:g.140957883T>C	GRCh38
NC_000003.11:g.140676725T>C , CM000665.1:g.140676725T>C	GRCh37
NC_000003.10:g.142159415T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000324194.12:c.206+1192T>C MANE Select	ENSP00000320688.6:n.206+1192T>C
ENST00000648615.1:c.206+1192T>C	ENSP00000497436.1:n.206+1192T>C
ENST00000324194.10:c.206+1192T>C	ENSP00000320688.6:n.206+1192T>C
ENST00000393015.8:n.408+1192T>C
ENST00000446041.6:c.206+1192T>C	ENSP00000401938.2:n.206+1192T>C
ENST00000453248.6:c.206+1192T>C	ENSP00000391521.2:n.206+1192T>C
ENST00000502594.5:c.206+1192T>C	ENSP00000423319.1:n.206+1192T>C
ENST00000507429.5:c.206+1192T>C	ENSP00000421470.1:n.206+1192T>C
ENST00000512023.5:c.56+1192T>C	ENSP00000424505.1:n.56+1192T>C
ENST00000512506.5:c.56+1192T>C	ENSP00000423711.1:n.56+1192T>C
ENST00000513887.5:c.56+1192T>C	ENSP00000422265.1:n.56+1192T>C
ENST00000515813.1:n.393+1192T>C
ENST00000631654.1:c.206+1192T>C	ENSP00000487839.1:n.206+1192T>C
NM_001104647.1:c.206+1192T>C	NP_001098117.1:n.206+1192T>C
NM_018155.2:c.206+1192T>C	NP_060625.2:n.206+1192T>C
XM_011512951.1:c.302+1192T>C	XP_011511253.1:n.302+1192T>C
XM_011512953.1:c.302+1192T>C	XP_011511255.1:n.302+1192T>C
XR_924150.1:n.495+1192T>C
XR_924151.1:n.495+1192T>C
XR_924152.1:n.495+1192T>C
XR_924153.1:n.495+1192T>C
XR_924154.1:n.495+1192T>C
XR_924155.1:n.495+1192T>C
XR_924156.1:n.495+1192T>C
XR_924157.1:n.495+1192T>C
NM_001104647.3:c.206+1192T>C MANE Select	NP_001098117.1:n.206+1192T>C
NM_018155.3:c.206+1192T>C	NP_060625.2:n.206+1192T>C