Canonical Allele Identifier: CA436070439

Gene: SLC25A36

Linked Data

• MyVariant Identifiers: chr3:g.140682029T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.140963187T>G , CM000665.2:g.140963187T>G	GRCh38
NC_000003.11:g.140682029T>G , CM000665.1:g.140682029T>G	GRCh37
NC_000003.10:g.142164719T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324194.12:c.345T>G MANE Select	ENSP00000320688.6:p.Pro115=
ENST00000648615.1:c.345T>G	ENSP00000497436.1:p.Pro115=
ENST00000324194.10:c.345T>G	ENSP00000320688.6:p.Pro115=
ENST00000393015.8:n.547T>G
ENST00000446041.6:c.345T>G	ENSP00000401938.2:p.Pro115=
ENST00000453248.6:c.267T>G	ENSP00000391521.2:p.Pro89=
ENST00000502594.5:c.345T>G	ENSP00000423319.1:p.Pro115=
ENST00000507429.5:c.345T>G	ENSP00000421470.1:p.Pro115=
ENST00000512023.5:c.195T>G	ENSP00000424505.1:p.Pro65=
ENST00000512506.5:c.195T>G	ENSP00000423711.1:p.Pro65=
ENST00000513887.5:c.117T>G	ENSP00000422265.1:p.Pro39=
ENST00000515813.1:n.454T>G
ENST00000631654.1:c.345T>G	ENSP00000487839.1:p.Pro115=
NM_001104647.1:c.345T>G	NP_001098117.1:p.Pro115=
NM_018155.2:c.345T>G	NP_060625.2:p.Pro115=
XM_006713685.2:c.-762T>G	XP_006713748.1:n.-762T>G
XM_011512951.1:c.441T>G	XP_011511253.1:p.Pro147=
XM_011512952.1:c.-110T>G	XP_011511254.1:n.-110T>G
XM_011512953.1:c.441T>G	XP_011511255.1:p.Pro147=
XR_924150.1:n.634T>G
XR_924151.1:n.634T>G
XR_924152.1:n.634T>G
XR_924153.1:n.634T>G
XR_924154.1:n.634T>G
XR_924155.1:n.634T>G
XR_924156.1:n.634T>G
XR_924157.1:n.634T>G
NM_001104647.3:c.345T>G MANE Select	NP_001098117.1:p.Pro115=
NM_018155.3:c.345T>G	NP_060625.2:p.Pro115=