Canonical Allele Identifier: CA13436616
Gene: SYT9 HGNC NCBI
SYT9-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.7443141T>C , CM000673.2:g.7443141T>C GRCh38
NC_000011.9:g.7464372T>C , CM000673.1:g.7464372T>C GRCh37
NC_000011.8:g.7420948T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000318881.11:c.1467+22506T>C (SYT9) MANE Select ENSP00000324419.6:n.1467+22506T>C
ENST00000318881.10:c.1467+22506T>C (SYT9) ENSP00000324419.6:n.1467+22506T>C
ENST00000524820.6:c.*686-1048T>C (SYT9) ENSP00000432141.2:n.*686-1048T>C
ENST00000532592.1:c.*398+22506T>C (SYT9) ENSP00000434558.1:n.*398+22506T>C
NM_175733.3:c.1467+22506T>C (SYT9) NP_783860.1:n.1467+22506T>C
NR_103855.1:n.416-1422A>G (SYT9-AS1)
XM_005252795.2:c.1468-10860T>C (SYT9) XP_005252852.1:n.1468-10860T>C
XM_011519900.1:c.1468-8347T>C (SYT9) XP_011518202.1:n.1468-8347T>C
XM_011519901.1:c.1468-8347T>C (SYT9) XP_011518203.1:n.1468-8347T>C
XM_011519902.1:c.1372-8347T>C (SYT9) XP_011518204.1:n.1372-8347T>C
XM_011519900.2:c.1468-8347T>C (SYT9) XP_011518202.1:n.1468-8347T>C
XM_011519901.2:c.1468-8347T>C (SYT9) XP_011518203.1:n.1468-8347T>C
XM_011519902.2:c.1372-8347T>C (SYT9) XP_011518204.1:n.1372-8347T>C
XR_001747772.1:n.1677+22506T>C (SYT9)
XR_001747773.1:n.1678-8347T>C (SYT9)
NM_175733.4:c.1467+22506T>C (SYT9) MANE Select NP_783860.1:n.1467+22506T>C
Search 100 bp 5'
Search 100 bp 3'