Canonical Allele Identifier: CA393452203
Community Standard Title: NM_001145358.2(SIN3A):c.474-1G>A
Gene: SIN3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.75413046C>T , CM000677.2:g.75413046C>T GRCh38
NC_000015.9:g.75705387C>T , CM000677.1:g.75705387C>T GRCh37
NC_000015.8:g.73492440C>T NCBI36
NG_052855.1:g.47738G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001145358.2:c.474-1G>A MANE Select NP_001138830.1:n.474-1G>A
ENST00000394947.8:c.474-1G>A MANE Select ENSP00000378402.3:n.474-1G>A
NM_001145357.1:c.474-1G>A NP_001138829.1:n.474-1G>A
NM_001145357.2:c.474-1G>A NP_001138829.1:n.474-1G>A
NM_001145358.1:c.474-1G>A NP_001138830.1:n.474-1G>A
NM_015477.2:c.474-1G>A NP_056292.1:n.474-1G>A
NM_015477.3:c.474-1G>A NP_056292.1:n.474-1G>A
ENST00000360439.8:c.474-1G>A ENSP00000353622.4:n.474-1G>A
ENST00000394947.7:c.474-1G>A ENSP00000378402.3:n.474-1G>A
ENST00000394949.8:c.474-1G>A ENSP00000378403.4:n.474-1G>A
ENST00000564778.5:c.474-1G>A ENSP00000455204.1:n.474-1G>A
ENST00000564778.6:c.474-1G>A ENSP00000455204.2:n.474-1G>A
ENST00000565264.2:c.474-1G>A ENSP00000454296.2:n.474-1G>A
ENST00000704304.1:c.*428-1G>A ENSP00000515828.1:n.*428-1G>A
ENST00000704305.1:c.584-1G>A ENSP00000515829.1:n.584-1G>A
ENST00000704310.1:c.474-1G>A ENSP00000515832.1:n.474-1G>A
ENST00000704312.1:c.474-1G>A ENSP00000515834.1:n.474-1G>A
XM_006720465.2:c.474-1G>A XP_006720528.1:n.474-1G>A
XM_006720465.3:c.474-1G>A XP_006720528.1:n.474-1G>A
XM_006720466.2:c.474-1G>A XP_006720529.1:n.474-1G>A
XM_006720466.3:c.474-1G>A XP_006720529.1:n.474-1G>A
XM_006720467.2:c.474-1G>A XP_006720530.1:n.474-1G>A
XM_006720467.3:c.474-1G>A XP_006720530.1:n.474-1G>A
XM_024449896.1:c.474-1G>A XP_024305664.1:n.474-1G>A