Canonical Allele Identifier: CA2506065370

Gene: SYT9

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.7345937_7345954del , CM000673.2:g.7345937_7345954del	GRCh38
NC_000011.9:g.7367168_7367185del , CM000673.1:g.7367168_7367185del	GRCh37
NC_000011.8:g.7323744_7323761del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318881.11:c.1044+31996_1044+32013del MANE Select	ENSP00000324419.6:n.1044+31996_1044+32013del
ENST00000318881.10:c.1044+31996_1044+32013del	ENSP00000324419.6:n.1044+31996_1044+32013del
ENST00000524820.6:c.*141+31600_*141+31617del	ENSP00000432141.2:n.*141+31600_*141+31617del
ENST00000532592.1:c.497+42547_497+42564del	ENSP00000434558.1:n.497+42547_497+42564del
NM_175733.3:c.1044+31996_1044+32013del	NP_783860.1:n.1044+31996_1044+32013del
XM_005252795.2:c.1044+31996_1044+32013del	XP_005252852.1:n.1044+31996_1044+32013del
XM_011519900.1:c.1044+31996_1044+32013del	XP_011518202.1:n.1044+31996_1044+32013del
XM_011519901.1:c.1044+31996_1044+32013del	XP_011518203.1:n.1044+31996_1044+32013del
XM_011519902.1:c.948+31996_948+32013del	XP_011518204.1:n.948+31996_948+32013del
XM_011519903.1:c.1044+31996_1044+32013del	XP_011518205.1:n.1044+31996_1044+32013del
XM_011519904.1:c.1044+31996_1044+32013del	XP_011518206.1:n.1044+31996_1044+32013del
XM_011519905.1:c.1044+31996_1044+32013del	XP_011518207.1:n.1044+31996_1044+32013del
XM_011519900.2:c.1044+31996_1044+32013del	XP_011518202.1:n.1044+31996_1044+32013del
XM_011519901.2:c.1044+31996_1044+32013del	XP_011518203.1:n.1044+31996_1044+32013del
XM_011519902.2:c.948+31996_948+32013del	XP_011518204.1:n.948+31996_948+32013del
XM_011519904.2:c.1044+31996_1044+32013del	XP_011518206.1:n.1044+31996_1044+32013del
XR_001747772.1:n.1259+31996_1259+32013del
XR_001747773.1:n.1259+31996_1259+32013del
NM_175733.4:c.1044+31996_1044+32013del MANE Select	NP_783860.1:n.1044+31996_1044+32013del