Canonical Allele Identifier: CA2504907423

Gene: SYT9

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.7345934_7345935insTTT , CM000673.2:g.7345934_7345935insTTT	GRCh38
NC_000011.9:g.7367165_7367166insTTT , CM000673.1:g.7367165_7367166insTTT	GRCh37
NC_000011.8:g.7323741_7323742insTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000318881.11:c.1044+31993_1044+31994insTTT MANE Select	ENSP00000324419.6:n.1044+31993_1044+31994insTTT
ENST00000318881.10:c.1044+31993_1044+31994insTTT	ENSP00000324419.6:n.1044+31993_1044+31994insTTT
ENST00000524820.6:c.*141+31597_*141+31598insTTT	ENSP00000432141.2:n.*141+31597_*141+31598insTTT
ENST00000532592.1:c.497+42544_497+42545insTTT	ENSP00000434558.1:n.497+42544_497+42545insTTT
NM_175733.3:c.1044+31993_1044+31994insTTT	NP_783860.1:n.1044+31993_1044+31994insTTT
XM_005252795.2:c.1044+31993_1044+31994insTTT	XP_005252852.1:n.1044+31993_1044+31994insTTT
XM_011519900.1:c.1044+31993_1044+31994insTTT	XP_011518202.1:n.1044+31993_1044+31994insTTT
XM_011519901.1:c.1044+31993_1044+31994insTTT	XP_011518203.1:n.1044+31993_1044+31994insTTT
XM_011519902.1:c.948+31993_948+31994insTTT	XP_011518204.1:n.948+31993_948+31994insTTT
XM_011519903.1:c.1044+31993_1044+31994insTTT	XP_011518205.1:n.1044+31993_1044+31994insTTT
XM_011519904.1:c.1044+31993_1044+31994insTTT	XP_011518206.1:n.1044+31993_1044+31994insTTT
XM_011519905.1:c.1044+31993_1044+31994insTTT	XP_011518207.1:n.1044+31993_1044+31994insTTT
XM_011519900.2:c.1044+31993_1044+31994insTTT	XP_011518202.1:n.1044+31993_1044+31994insTTT
XM_011519901.2:c.1044+31993_1044+31994insTTT	XP_011518203.1:n.1044+31993_1044+31994insTTT
XM_011519902.2:c.948+31993_948+31994insTTT	XP_011518204.1:n.948+31993_948+31994insTTT
XM_011519904.2:c.1044+31993_1044+31994insTTT	XP_011518206.1:n.1044+31993_1044+31994insTTT
XR_001747772.1:n.1259+31993_1259+31994insTTT
XR_001747773.1:n.1259+31993_1259+31994insTTT
NM_175733.4:c.1044+31993_1044+31994insTTT MANE Select	NP_783860.1:n.1044+31993_1044+31994insTTT