Canonical Allele Identifier: CA1950591758
Gene: SYT9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.7345963G= , CM000673.2:g.7345963G= GRCh38
NC_000011.9:g.7367194G= , CM000673.1:g.7367194G= GRCh37
NC_000011.8:g.7323770G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000318881.11:c.1044+32022G= MANE Select ENSP00000324419.6:n.1044+32022G=
ENST00000318881.10:c.1044+32022G= ENSP00000324419.6:n.1044+32022G=
ENST00000524820.6:c.*141+31626G= ENSP00000432141.2:n.*141+31626G=
ENST00000532592.1:c.497+42573G= ENSP00000434558.1:n.497+42573G=
NM_175733.3:c.1044+32022G= NP_783860.1:n.1044+32022G=
XM_005252795.2:c.1044+32022G= XP_005252852.1:n.1044+32022G=
XM_011519900.1:c.1044+32022G= XP_011518202.1:n.1044+32022G=
XM_011519901.1:c.1044+32022G= XP_011518203.1:n.1044+32022G=
XM_011519902.1:c.948+32022G= XP_011518204.1:n.948+32022G=
XM_011519903.1:c.1044+32022G= XP_011518205.1:n.1044+32022G=
XM_011519904.1:c.1044+32022G= XP_011518206.1:n.1044+32022G=
XM_011519905.1:c.1044+32022G= XP_011518207.1:n.1044+32022G=
XM_011519900.2:c.1044+32022G= XP_011518202.1:n.1044+32022G=
XM_011519901.2:c.1044+32022G= XP_011518203.1:n.1044+32022G=
XM_011519902.2:c.948+32022G= XP_011518204.1:n.948+32022G=
XM_011519904.2:c.1044+32022G= XP_011518206.1:n.1044+32022G=
XR_001747772.1:n.1259+32022G=
XR_001747773.1:n.1259+32022G=
NM_175733.4:c.1044+32022G= MANE Select NP_783860.1:n.1044+32022G=