Canonical Allele Identifier: CA35582645

Gene: SYT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202604279dup , CM000663.2:g.202604279dup	GRCh38
NC_000001.10:g.202573407dup , CM000663.1:g.202573407dup	GRCh37
NC_000001.9:g.200840030dup	NCBI36
NG_041776.1:g.111152dup

Transcript Alleles

HGVS	Amino-acid Change
NM_177402.5:c.345+183dup MANE Select	NP_796376.2:n.345+183dup
ENST00000367268.5:c.345+183dup MANE Select	ENSP00000356237.4:n.345+183dup
NM_001136504.1:c.345+183dup	NP_001129976.1:n.345+183dup
NM_177402.4:c.345+183dup	NP_796376.2:n.345+183dup
ENST00000367267.5:c.345+183dup	ENSP00000356236.1:n.345+183dup
ENST00000367268.4:c.345+183dup	ENSP00000356237.4:n.345+183dup
XM_011509191.1:c.345+183dup	XP_011507493.1:n.345+183dup
XM_011509192.1:c.345+183dup	XP_011507494.1:n.345+183dup
XM_011509192.2:c.345+183dup	XP_011507494.1:n.345+183dup
XM_017000309.2:c.516+183dup	XP_016855798.1:n.516+183dup
XM_017000310.2:c.516+183dup	XP_016855799.1:n.516+183dup
XM_017000311.2:c.345+183dup	XP_016855800.1:n.345+183dup
XM_017000312.1:c.345+183dup	XP_016855801.1:n.345+183dup
XM_017000313.1:c.345+183dup	XP_016855802.1:n.345+183dup