Canonical Allele Identifier: CA10586184
Gene: SIN3A HGNC NCBI
ClinVar RCV:
ClinVar Variation:
COSMIC:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.75380702G>A , CM000677.2:g.75380702G>A GRCh38
NC_000015.9:g.75673043G>A , CM000677.1:g.75673043G>A GRCh37
NC_000015.8:g.73460096G>A NCBI36
NG_052855.1:g.80082C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000564778.6:c.3310C>T ENSP00000455204.2:p.Arg1104Ter
ENST00000565264.2:c.3310C>T ENSP00000454296.2:p.Arg1104Ter
ENST00000704302.1:c.2632C>T ENSP00000515826.1:p.Arg878Ter
ENST00000704304.1:c.*3264C>T ENSP00000515828.1:n.*3264C>T
ENST00000704305.1:c.3420C>T ENSP00000515829.1:n.3420C>T
ENST00000704310.1:c.3325C>T ENSP00000515832.1:p.Arg1109Ter
ENST00000704311.1:c.2207C>T
ENST00000704312.1:c.3310C>T ENSP00000515834.1:p.Arg1104Ter
ENST00000394947.8:c.3310C>T MANE Select ENSP00000378402.3:p.Arg1104Ter
ENST00000360439.8:c.3310C>T ENSP00000353622.4:p.Arg1104Ter
ENST00000394947.7:c.3310C>T ENSP00000378402.3:p.Arg1104Ter
ENST00000394949.8:c.3310C>T ENSP00000378403.4:p.Arg1104Ter
ENST00000570124.1:n.387C>T
NM_001145357.1:c.3310C>T NP_001138829.1:p.Arg1104Ter
NM_001145358.1:c.3310C>T NP_001138830.1:p.Arg1104Ter
NM_015477.2:c.3310C>T NP_056292.1:p.Arg1104Ter
XM_006720465.2:c.3310C>T XP_006720528.1:p.Arg1104Ter
XM_006720466.2:c.3310C>T XP_006720529.1:p.Arg1104Ter
XM_006720467.2:c.3310C>T XP_006720530.1:p.Arg1104Ter
XM_006720465.3:c.3310C>T XP_006720528.1:p.Arg1104Ter
XM_006720466.3:c.3310C>T XP_006720529.1:p.Arg1104Ter
XM_006720467.3:c.3310C>T XP_006720530.1:p.Arg1104Ter
XM_024449896.1:c.3310C>T XP_024305664.1:p.Arg1104Ter
NM_001145357.2:c.3310C>T NP_001138829.1:p.Arg1104Ter
NM_001145358.2:c.3310C>T MANE Select NP_001138830.1:p.Arg1104Ter
NM_015477.3:c.3310C>T NP_056292.1:p.Arg1104Ter