Canonical Allele Identifier: CA2048676463

Gene: SYT1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.79191060T= , CM000674.2:g.79191060T=	GRCh38
NC_000012.11:g.79584840T= , CM000674.1:g.79584840T=	GRCh37
NC_000012.10:g.78108971T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000704696.1:c.-17-26443T=	ENSP00000515993.1:n.-17-26443T=
ENST00000704697.1:c.-17-26443T=	ENSP00000515994.1:n.-17-26443T=
ENST00000704698.1:c.-24+213129T=	ENSP00000515995.1:n.-24+213129T=
ENST00000704699.1:c.-17-26443T=	ENSP00000515996.1:n.-17-26443T=
ENST00000704700.1:c.-17-26443T=	ENSP00000515997.1:n.-17-26443T=
ENST00000704701.1:c.-17-26443T=	ENSP00000515998.1:n.-17-26443T=
ENST00000704702.1:c.-17-26443T=	ENSP00000515999.1:n.-17-26443T=
ENST00000704703.1:c.2-94727T=	ENSP00000516000.1:n.2-94727T=
ENST00000704704.1:c.-17-26443T=	ENSP00000516001.1:n.-17-26443T=
ENST00000704705.1:c.-17-26443T=	ENSP00000516002.1:n.-17-26443T=
ENST00000704706.1:c.-17-26443T=	ENSP00000516003.1:n.-17-26443T=
ENST00000704707.1:c.-17-26443T=	ENSP00000516004.1:n.-17-26443T=
ENST00000704708.1:c.-17-26443T=	ENSP00000516005.1:n.-17-26443T=
ENST00000704709.1:c.-18+8488T=	ENSP00000516006.1:n.-18+8488T=
ENST00000704710.1:c.-18+8488T=	ENSP00000516007.1:n.-18+8488T=
ENST00000704711.1:c.-17-26443T=	ENSP00000516008.1:n.-17-26443T=
ENST00000704714.1:c.-17-26443T=	ENSP00000516009.1:n.-17-26443T=
ENST00000704715.1:c.-17-26443T=	ENSP00000516010.1:n.-17-26443T=
ENST00000704716.1:c.-17-26443T=	ENSP00000516011.1:n.-17-26443T=
ENST00000704717.1:c.-17-26443T=	ENSP00000516012.1:n.-17-26443T=
ENST00000704718.1:c.-17-26443T=	ENSP00000516013.1:n.-17-26443T=
ENST00000704719.1:c.-87-7613T=	ENSP00000516014.1:n.-87-7613T=
ENST00000261205.9:c.-17-26443T= MANE Select	ENSP00000261205.4:n.-17-26443T=
ENST00000261205.8:c.-17-26443T=	ENSP00000261205.4:n.-17-26443T=
ENST00000393240.7:c.-17-26443T=	ENSP00000376932.3:n.-17-26443T=
ENST00000446242.3:c.-17-26443T=	ENSP00000401559.2:n.-17-26443T=
ENST00000457153.6:c.-17-26443T=	ENSP00000391056.2:n.-17-26443T=
ENST00000547046.5:c.-17-26443T=	ENSP00000448964.1:n.-17-26443T=
ENST00000549454.5:n.569-26443T=
ENST00000549671.5:c.-17-26443T=	ENSP00000450321.1:n.-17-26443T=
ENST00000551304.5:c.-17-26443T=	ENSP00000447656.1:n.-17-26443T=
ENST00000552074.5:c.-17-26443T=	ENSP00000447035.1:n.-17-26443T=
ENST00000552624.5:c.-17-26443T=	ENSP00000448861.1:n.-17-26443T=
ENST00000552744.5:c.-17-26443T=	ENSP00000447575.1:n.-17-26443T=
NM_001135805.1:c.-17-26443T=	NP_001129277.1:n.-17-26443T=
NM_001135806.1:c.-17-26443T=	NP_001129278.1:n.-17-26443T=
NM_001291901.1:c.-17-26443T=	NP_001278830.1:n.-17-26443T=
NM_005639.2:c.-17-26443T=	NP_005630.1:n.-17-26443T=
XM_005269113.2:c.-17-26443T=	XP_005269170.1:n.-17-26443T=
XM_006719576.1:c.-17-26443T=	XP_006719639.1:n.-17-26443T=
XM_011538710.1:c.-17-26443T=	XP_011537012.1:n.-17-26443T=
XM_005269113.3:c.-17-26443T=	XP_005269170.1:n.-17-26443T=
XM_011538710.2:c.-17-26443T=	XP_011537012.1:n.-17-26443T=
NM_005639.3:c.-17-26443T= MANE Select	NP_005630.1:n.-17-26443T=
NM_001135805.2:c.-17-26443T=	NP_001129277.1:n.-17-26443T=
NM_001135806.2:c.-17-26443T=	NP_001129278.1:n.-17-26443T=
NM_001291901.2:c.-17-26443T=	NP_001278830.1:n.-17-26443T=