Canonical Allele Identifier: CA1675912249

Gene: SYNJ2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158014540A>C , CM000668.2:g.158014540A>C	GRCh38
NC_000006.11:g.158435572A>C , CM000668.1:g.158435572A>C	GRCh37
NC_000006.10:g.158355560A>C	NCBI36
NG_029907.1:g.37685A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355585.9:c.128-2664A>C MANE Select	ENSP00000347792.4:n.128-2664A>C
ENST00000367113.5:c.52-2664A>C
ENST00000640338.1:c.128-2664A>C	ENSP00000492532.1:n.128-2664A>C
ENST00000355585.8:c.128-2664A>C	ENSP00000347792.4:n.128-2664A>C
ENST00000367113.4:c.52-2664A>C
NM_003898.3:c.128-2664A>C	NP_003889.1:n.128-2664A>C
XM_006715592.2:c.128-2664A>C	XP_006715655.1:n.128-2664A>C
XM_011536224.1:c.128-2664A>C	XP_011534526.1:n.128-2664A>C
XM_011536225.1:c.-584-2664A>C	XP_011534527.1:n.-584-2664A>C
XM_011536227.1:c.128-2664A>C	XP_011534529.1:n.128-2664A>C
XM_011536229.1:c.128-2664A>C	XP_011534531.1:n.128-2664A>C
XM_011536230.1:c.128-2664A>C	XP_011534532.1:n.128-2664A>C
XR_245556.1:n.234-2664A>C
XM_006715592.3:c.128-2664A>C	XP_006715655.1:n.128-2664A>C
XM_011536227.2:c.128-2664A>C	XP_011534529.1:n.128-2664A>C
XM_011536230.2:c.128-2664A>C	XP_011534532.1:n.128-2664A>C
NM_003898.4:c.128-2664A>C MANE Select	NP_003889.1:n.128-2664A>C