Canonical Allele Identifier: CA393499014

Gene: SIN3A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.75401851C>A , CM000677.2:g.75401851C>A	GRCh38
NC_000015.9:g.75694192C>A , CM000677.1:g.75694192C>A	GRCh37
NC_000015.8:g.73481245C>A	NCBI36
NG_052855.1:g.58933G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001145358.2:c.1526+1G>T MANE Select	NP_001138830.1:n.1526+1G>T
ENST00000394947.8:c.1526+1G>T MANE Select	ENSP00000378402.3:n.1526+1G>T
NM_001145357.1:c.1526+1G>T	NP_001138829.1:n.1526+1G>T
NM_001145357.2:c.1526+1G>T	NP_001138829.1:n.1526+1G>T
NM_001145358.1:c.1526+1G>T	NP_001138830.1:n.1526+1G>T
NM_015477.2:c.1526+1G>T	NP_056292.1:n.1526+1G>T
NM_015477.3:c.1526+1G>T	NP_056292.1:n.1526+1G>T
ENST00000360439.8:c.1526+1G>T	ENSP00000353622.4:n.1526+1G>T
ENST00000394947.7:c.1526+1G>T	ENSP00000378402.3:n.1526+1G>T
ENST00000394949.8:c.1526+1G>T	ENSP00000378403.4:n.1526+1G>T
ENST00000564778.6:c.1526+1G>T	ENSP00000455204.2:n.1526+1G>T
ENST00000565264.2:c.1526+1G>T	ENSP00000454296.2:n.1526+1G>T
ENST00000704302.1:c.848+1G>T	ENSP00000515826.1:n.848+1G>T
ENST00000704304.1:c.*1480+1G>T	ENSP00000515828.1:n.*1480+1G>T
ENST00000704305.1:c.1636+1G>T	ENSP00000515829.1:n.1636+1G>T
ENST00000704310.1:c.1526+1G>T	ENSP00000515832.1:n.1526+1G>T
ENST00000704311.1:c.306+1G>T
ENST00000704312.1:c.1526+1G>T	ENSP00000515834.1:n.1526+1G>T
XM_006720465.2:c.1526+1G>T	XP_006720528.1:n.1526+1G>T
XM_006720465.3:c.1526+1G>T	XP_006720528.1:n.1526+1G>T
XM_006720466.2:c.1526+1G>T	XP_006720529.1:n.1526+1G>T
XM_006720466.3:c.1526+1G>T	XP_006720529.1:n.1526+1G>T
XM_006720467.2:c.1526+1G>T	XP_006720530.1:n.1526+1G>T
XM_006720467.3:c.1526+1G>T	XP_006720530.1:n.1526+1G>T
XM_024449896.1:c.1526+1G>T	XP_024305664.1:n.1526+1G>T