Canonical Allele Identifier: CA393490462

Gene: SIN3A

Linked Data

• MyVariant Identifiers: chr15:g.75684656C>A (hg19) ; chr15:g.75392315C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.75392315C>A , CM000677.2:g.75392315C>A	GRCh38
NC_000015.9:g.75684656C>A , CM000677.1:g.75684656C>A	GRCh37
NC_000015.8:g.73471709C>A	NCBI36
NG_052855.1:g.68469G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000564778.6:c.2778G>T	ENSP00000455204.2:p.Trp926Cys
ENST00000565264.2:c.2778G>T	ENSP00000454296.2:p.Trp926Cys
ENST00000704302.1:c.2100G>T	ENSP00000515826.1:p.Trp700Cys
ENST00000704304.1:c.*2732G>T	ENSP00000515828.1:n.*2732G>T
ENST00000704305.1:c.2888G>T	ENSP00000515829.1:n.2888G>T
ENST00000704310.1:c.2778G>T	ENSP00000515832.1:p.Trp926Cys
ENST00000704311.1:c.1675G>T
ENST00000704312.1:c.2778G>T	ENSP00000515834.1:p.Trp926Cys
ENST00000394947.8:c.2778G>T MANE Select	ENSP00000378402.3:p.Trp926Cys
ENST00000360439.8:c.2778G>T	ENSP00000353622.4:p.Trp926Cys
ENST00000394947.7:c.2778G>T	ENSP00000378402.3:p.Trp926Cys
ENST00000394949.8:c.2778G>T	ENSP00000378403.4:p.Trp926Cys
NM_001145357.1:c.2778G>T	NP_001138829.1:p.Trp926Cys
NM_001145358.1:c.2778G>T	NP_001138830.1:p.Trp926Cys
NM_015477.2:c.2778G>T	NP_056292.1:p.Trp926Cys
XM_006720465.2:c.2778G>T	XP_006720528.1:p.Trp926Cys
XM_006720466.2:c.2778G>T	XP_006720529.1:p.Trp926Cys
XM_006720467.2:c.2778G>T	XP_006720530.1:p.Trp926Cys
XM_006720465.3:c.2778G>T	XP_006720528.1:p.Trp926Cys
XM_006720466.3:c.2778G>T	XP_006720529.1:p.Trp926Cys
XM_006720467.3:c.2778G>T	XP_006720530.1:p.Trp926Cys
XM_024449896.1:c.2778G>T	XP_024305664.1:p.Trp926Cys
NM_001145357.2:c.2778G>T	NP_001138829.1:p.Trp926Cys
NM_001145358.2:c.2778G>T MANE Select	NP_001138830.1:p.Trp926Cys
NM_015477.3:c.2778G>T	NP_056292.1:p.Trp926Cys