Canonical Allele Identifier: CA1346039346

Gene: SYN2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.12188056_12188060delinsGACTC , CM000665.2:g.12188056_12188060delinsGACTC	GRCh38
NC_000003.11:g.12229556_12229560delinsGACTC , CM000665.1:g.12229556_12229560delinsGACTC	GRCh37
NC_000003.10:g.12204556_12204560delinsGACTC	NCBI36
NG_011728.2:g.188669_188673delinsGACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000621198.5:c.1613+444_1613+448delinsGACTC MANE Select	ENSP00000480050.1:n.1613+444_1613+448delinsGACTC
ENST00000439861.5:n.1232+444_1232+448delinsGACTC
ENST00000621198.4:c.1613+444_1613+448delinsGACTC	ENSP00000480050.1:n.1613+444_1613+448delinsGACTC
NM_133625.4:c.1613+444_1613+448delinsGACTC	NP_598328.1:n.1613+444_1613+448delinsGACTC
XM_006713312.2:c.1130+444_1130+448delinsGACTC	XP_006713375.1:n.1130+444_1130+448delinsGACTC
XM_006713313.2:c.842+444_842+448delinsGACTC	XP_006713376.1:n.842+444_842+448delinsGACTC
XM_006713312.4:c.1130+444_1130+448delinsGACTC	XP_006713375.1:n.1130+444_1130+448delinsGACTC
XM_017007087.1:c.941+444_941+448delinsGACTC	XP_016862576.1:n.941+444_941+448delinsGACTC
NM_133625.5:c.1613+444_1613+448delinsGACTC	NP_598328.1:n.1613+444_1613+448delinsGACTC
NM_133625.6:c.1613+444_1613+448delinsGACTC MANE Select	NP_598328.1:n.1613+444_1613+448delinsGACTC