Canonical Allele Identifier: CA680054787

Gene: SYT9

Linked Data

• dbSNP Id: rs1336816905
• gnomAD v3: 11-7345827-AGAG-A
• gnomAD v4: 11-7345827-AGAG-A
• MyVariant Identifiers: chr11:g.7367059_7367061del (hg19) ; chr11:g.7345828_7345830del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.7345833_7345835del , CM000673.2:g.7345833_7345835del	GRCh38
NC_000011.9:g.7367064_7367066del , CM000673.1:g.7367064_7367066del	GRCh37
NC_000011.8:g.7323640_7323642del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000318881.11:c.1044+31892_1044+31894del MANE Select	ENSP00000324419.6:n.1044+31892_1044+31894...
ENST00000318881.10:c.1044+31892_1044+31894del	ENSP00000324419.6:n.1044+31892_1044+31894...
ENST00000524820.6:c.*141+31496_*141+31498del	ENSP00000432141.2:n.*141+31496_*141+31498...
ENST00000532592.1:c.497+42443_497+42445del	ENSP00000434558.1:n.497+42443_497+42445de...
NM_175733.3:c.1044+31892_1044+31894del	NP_783860.1:n.1044+31892_1044+31894del
XM_005252795.2:c.1044+31892_1044+31894del	XP_005252852.1:n.1044+31892_1044+31894del...
XM_011519900.1:c.1044+31892_1044+31894del	XP_011518202.1:n.1044+31892_1044+31894del...
XM_011519901.1:c.1044+31892_1044+31894del	XP_011518203.1:n.1044+31892_1044+31894del...
XM_011519902.1:c.948+31892_948+31894del	XP_011518204.1:n.948+31892_948+31894del
XM_011519903.1:c.1044+31892_1044+31894del	XP_011518205.1:n.1044+31892_1044+31894del...
XM_011519904.1:c.1044+31892_1044+31894del	XP_011518206.1:n.1044+31892_1044+31894del...
XM_011519905.1:c.1044+31892_1044+31894del	XP_011518207.1:n.1044+31892_1044+31894del...
XM_011519900.2:c.1044+31892_1044+31894del	XP_011518202.1:n.1044+31892_1044+31894del...
XM_011519901.2:c.1044+31892_1044+31894del	XP_011518203.1:n.1044+31892_1044+31894del...
XM_011519902.2:c.948+31892_948+31894del	XP_011518204.1:n.948+31892_948+31894del
XM_011519904.2:c.1044+31892_1044+31894del	XP_011518206.1:n.1044+31892_1044+31894del...
XR_001747772.1:n.1259+31892_1259+31894del
XR_001747773.1:n.1259+31892_1259+31894del
NM_175733.4:c.1044+31892_1044+31894del MANE Select	NP_783860.1:n.1044+31892_1044+31894del