Canonical Allele Identifier: CA2840850724
Gene: SYT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.202596975dup , CM000663.2:g.202596975dup GRCh38
NC_000001.10:g.202566103dup , CM000663.1:g.202566103dup GRCh37
NC_000001.9:g.200832726dup NCBI36
NG_041776.1:g.118452dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367268.5:c.1054-9dup MANE Select ENSP00000356237.4:n.1054-9dup
ENST00000367267.5:c.1054-9dup ENSP00000356236.1:n.1054-9dup
ENST00000367268.4:c.1054-9dup ENSP00000356237.4:n.1054-9dup
NM_001136504.1:c.1054-9dup NP_001129976.1:n.1054-9dup
NM_177402.4:c.1054-9dup NP_796376.2:n.1054-9dup
XM_011509192.1:c.1063-9dup XP_011507494.1:n.1063-9dup
XM_011509192.2:c.1063-9dup XP_011507494.1:n.1063-9dup
XM_017000309.2:c.1234-9dup XP_016855798.1:n.1234-9dup
XM_017000310.2:c.1225-9dup XP_016855799.1:n.1225-9dup
XM_017000311.2:c.1063-9dup XP_016855800.1:n.1063-9dup
XM_017000312.1:c.1063-9dup XP_016855801.1:n.1063-9dup
XM_017000313.1:c.1054-9dup XP_016855802.1:n.1054-9dup
NM_177402.5:c.1054-9dup MANE Select NP_796376.2:n.1054-9dup