Canonical Allele Identifier: CA11556397

Gene: SIDT1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.113571621T>C , CM000665.2:g.113571621T>C	GRCh38
NC_000003.11:g.113290468T>C , CM000665.1:g.113290468T>C	GRCh37
NC_000003.10:g.114773158T>C	NCBI36
NG_054720.1:g.44848T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264852.9:c.515+3911T>C MANE Select	ENSP00000264852.4:n.515+3911T>C
ENST00000264852.8:c.515+3911T>C	ENSP00000264852.4:n.515+3911T>C
ENST00000393830.4:c.515+3911T>C	ENSP00000377416.4:n.515+3911T>C
ENST00000491730.5:n.982+3911T>C
NM_001308350.1:c.515+3911T>C	NP_001295279.1:n.515+3911T>C
NM_017699.2:c.515+3911T>C	NP_060169.2:n.515+3911T>C
XM_006713680.2:c.515+3911T>C	XP_006713743.1:n.515+3911T>C
XM_011512939.1:c.515+3911T>C	XP_011511241.1:n.515+3911T>C
XM_011512940.1:c.515+3911T>C	XP_011511242.1:n.515+3911T>C
XM_011512941.1:c.515+3911T>C	XP_011511243.1:n.515+3911T>C
XM_011512942.1:c.515+3911T>C	XP_011511244.1:n.515+3911T>C
XR_241500.1:n.1126+3911T>C
NM_001322294.1:c.515+3911T>C	NP_001309223.1:n.515+3911T>C
NM_001322295.1:c.515+3911T>C	NP_001309224.1:n.515+3911T>C
NM_001322296.1:c.515+3911T>C	NP_001309225.1:n.515+3911T>C
NM_001322297.1:c.62+3911T>C	NP_001309226.1:n.62+3911T>C
NM_001322298.1:c.-6+3911T>C	NP_001309227.1:n.-6+3911T>C
NM_001322299.1:c.-246+3911T>C	NP_001309228.1:n.-246+3911T>C
NM_001322300.1:c.-664+3911T>C	NP_001309229.1:n.-664+3911T>C
NR_136280.1:n.1246+3911T>C
NR_136281.1:n.1166+3911T>C
NR_136282.1:n.1166+3911T>C
NR_136283.1:n.1166+3911T>C
NR_136284.1:n.1166+3911T>C
NR_136285.1:n.1166+3911T>C
XM_011512939.3:c.515+3911T>C	XP_011511241.1:n.515+3911T>C
XM_011512941.3:c.515+3911T>C	XP_011511243.1:n.515+3911T>C
XM_017006664.2:c.515+3911T>C	XP_016862153.1:n.515+3911T>C
XM_017006665.2:c.62+3911T>C	XP_016862154.1:n.62+3911T>C
XM_017006666.1:c.-61+3911T>C	XP_016862155.1:n.-61+3911T>C
XR_001740185.2:n.1024+3911T>C
NM_001322294.2:c.515+3911T>C	NP_001309223.1:n.515+3911T>C
NM_001322295.2:c.515+3911T>C	NP_001309224.1:n.515+3911T>C
NM_001322296.2:c.515+3911T>C	NP_001309225.1:n.515+3911T>C
NM_001322297.2:c.62+3911T>C	NP_001309226.1:n.62+3911T>C
NM_001322298.2:c.-6+3911T>C	NP_001309227.1:n.-6+3911T>C
NM_001322299.2:c.-246+3911T>C	NP_001309228.1:n.-246+3911T>C
NM_001322300.2:c.-664+3911T>C	NP_001309229.1:n.-664+3911T>C
NM_017699.3:c.515+3911T>C MANE Select	NP_060169.2:n.515+3911T>C
NR_136280.2:n.1062+3911T>C
NR_136281.2:n.982+3911T>C
NR_136282.2:n.982+3911T>C
NR_136283.2:n.982+3911T>C
NR_136284.2:n.982+3911T>C
NR_136285.2:n.982+3911T>C
NM_001308350.2:c.515+3911T>C	NP_001295279.1:n.515+3911T>C