Canonical Allele Identifier: CA393490441

Gene: SIN3A

Linked Data

• MyVariant Identifiers: chr15:g.75684646C>T (hg19) ; chr15:g.75392305C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.75392305C>T , CM000677.2:g.75392305C>T	GRCh38
NC_000015.9:g.75684646C>T , CM000677.1:g.75684646C>T	GRCh37
NC_000015.8:g.73471699C>T	NCBI36
NG_052855.1:g.68479G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000564778.6:c.2788G>A	ENSP00000455204.2:p.Val930Met
ENST00000565264.2:c.2788G>A	ENSP00000454296.2:p.Val930Met
ENST00000704302.1:c.2110G>A	ENSP00000515826.1:p.Val704Met
ENST00000704304.1:c.*2742G>A	ENSP00000515828.1:n.*2742G>A
ENST00000704305.1:c.2898G>A	ENSP00000515829.1:n.2898G>A
ENST00000704310.1:c.2788G>A	ENSP00000515832.1:p.Val930Met
ENST00000704311.1:c.1685G>A
ENST00000704312.1:c.2788G>A	ENSP00000515834.1:p.Val930Met
ENST00000394947.8:c.2788G>A MANE Select	ENSP00000378402.3:p.Val930Met
ENST00000360439.8:c.2788G>A	ENSP00000353622.4:p.Val930Met
ENST00000394947.7:c.2788G>A	ENSP00000378402.3:p.Val930Met
ENST00000394949.8:c.2788G>A	ENSP00000378403.4:p.Val930Met
NM_001145357.1:c.2788G>A	NP_001138829.1:p.Val930Met
NM_001145358.1:c.2788G>A	NP_001138830.1:p.Val930Met
NM_015477.2:c.2788G>A	NP_056292.1:p.Val930Met
XM_006720465.2:c.2788G>A	XP_006720528.1:p.Val930Met
XM_006720466.2:c.2788G>A	XP_006720529.1:p.Val930Met
XM_006720467.2:c.2788G>A	XP_006720530.1:p.Val930Met
XM_006720465.3:c.2788G>A	XP_006720528.1:p.Val930Met
XM_006720466.3:c.2788G>A	XP_006720529.1:p.Val930Met
XM_006720467.3:c.2788G>A	XP_006720530.1:p.Val930Met
XM_024449896.1:c.2788G>A	XP_024305664.1:p.Val930Met
NM_001145357.2:c.2788G>A	NP_001138829.1:p.Val930Met
NM_001145358.2:c.2788G>A MANE Select	NP_001138830.1:p.Val930Met
NM_015477.3:c.2788G>A	NP_056292.1:p.Val930Met