Canonical Allele Identifier: CA393483425

Gene: SIN3A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.75372148G>C , CM000677.2:g.75372148G>C	GRCh38
NC_000015.9:g.75664489G>C , CM000677.1:g.75664489G>C	GRCh37
NC_000015.8:g.73451542G>C	NCBI36
NG_052855.1:g.88636C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001145358.2:c.3653C>G MANE Select	NP_001138830.1:p.Thr1218Ser
ENST00000394947.8:c.3653C>G MANE Select	ENSP00000378402.3:p.Thr1218Ser
NM_001145357.1:c.3653C>G	NP_001138829.1:p.Thr1218Ser
NM_001145357.2:c.3653C>G	NP_001138829.1:p.Thr1218Ser
NM_001145358.1:c.3653C>G	NP_001138830.1:p.Thr1218Ser
NM_015477.2:c.3653C>G	NP_056292.1:p.Thr1218Ser
NM_015477.3:c.3653C>G	NP_056292.1:p.Thr1218Ser
ENST00000360439.8:c.3653C>G	ENSP00000353622.4:p.Thr1218Ser
ENST00000394947.7:c.3653C>G	ENSP00000378402.3:p.Thr1218Ser
ENST00000394949.8:c.3653C>G	ENSP00000378403.4:p.Thr1218Ser
ENST00000564778.6:c.3653C>G	ENSP00000455204.2:p.Thr1218Ser
ENST00000565264.2:c.3653C>G	ENSP00000454296.2:p.Thr1218Ser
ENST00000566640.1:n.778C>G
ENST00000704302.1:c.3118C>G	ENSP00000515826.1:n.3118C>G
ENST00000704304.1:c.*3607C>G	ENSP00000515828.1:n.*3607C>G
ENST00000704305.1:c.3763C>G	ENSP00000515829.1:n.3763C>G
ENST00000704310.1:c.3668C>G	ENSP00000515832.1:p.Thr1223Ser
ENST00000704311.1:c.2550C>G
ENST00000704312.1:c.3653C>G	ENSP00000515834.1:p.Thr1218Ser
XM_006720465.2:c.3653C>G	XP_006720528.1:p.Thr1218Ser
XM_006720465.3:c.3653C>G	XP_006720528.1:p.Thr1218Ser
XM_006720466.2:c.3653C>G	XP_006720529.1:p.Thr1218Ser
XM_006720466.3:c.3653C>G	XP_006720529.1:p.Thr1218Ser
XM_006720467.2:c.3653C>G	XP_006720530.1:p.Thr1218Ser
XM_006720467.3:c.3653C>G	XP_006720530.1:p.Thr1218Ser
XM_024449896.1:c.3653C>G	XP_024305664.1:p.Thr1218Ser