Canonical Allele Identifier: CA1950591756
Gene: SYT9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.7345958T= , CM000673.2:g.7345958T= GRCh38
NC_000011.9:g.7367189T= , CM000673.1:g.7367189T= GRCh37
NC_000011.8:g.7323765T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000318881.11:c.1044+32017T= MANE Select ENSP00000324419.6:n.1044+32017T=
ENST00000318881.10:c.1044+32017T= ENSP00000324419.6:n.1044+32017T=
ENST00000524820.6:c.*141+31621T= ENSP00000432141.2:n.*141+31621T=
ENST00000532592.1:c.497+42568T= ENSP00000434558.1:n.497+42568T=
NM_175733.3:c.1044+32017T= NP_783860.1:n.1044+32017T=
XM_005252795.2:c.1044+32017T= XP_005252852.1:n.1044+32017T=
XM_011519900.1:c.1044+32017T= XP_011518202.1:n.1044+32017T=
XM_011519901.1:c.1044+32017T= XP_011518203.1:n.1044+32017T=
XM_011519902.1:c.948+32017T= XP_011518204.1:n.948+32017T=
XM_011519903.1:c.1044+32017T= XP_011518205.1:n.1044+32017T=
XM_011519904.1:c.1044+32017T= XP_011518206.1:n.1044+32017T=
XM_011519905.1:c.1044+32017T= XP_011518207.1:n.1044+32017T=
XM_011519900.2:c.1044+32017T= XP_011518202.1:n.1044+32017T=
XM_011519901.2:c.1044+32017T= XP_011518203.1:n.1044+32017T=
XM_011519902.2:c.948+32017T= XP_011518204.1:n.948+32017T=
XM_011519904.2:c.1044+32017T= XP_011518206.1:n.1044+32017T=
XR_001747772.1:n.1259+32017T=
XR_001747773.1:n.1259+32017T=
NM_175733.4:c.1044+32017T= MANE Select NP_783860.1:n.1044+32017T=