Canonical Allele Identifier: CA875955153

Gene: SYP

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49191412C>T , CM000685.2:g.49191412C>T	GRCh38
NC_000023.10:g.49047869C>T , CM000685.1:g.49047869C>T	GRCh37
NC_000023.9:g.48934813C>T	NCBI36
NG_012532.1:g.13793G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689634.1:n.2554G>A
ENST00000692723.1:n.972+21G>A
ENST00000263233.9:c.*4+21G>A MANE Select	ENSP00000263233.4:n.*4+21G>A
ENST00000263233.8:c.*4+21G>A	ENSP00000263233.4:n.*4+21G>A
ENST00000376303.6:c.*698+21G>A	ENSP00000365480.2:n.*698+21G>A
ENST00000472598.5:c.615+21G>A
ENST00000479808.5:c.*25G>A	ENSP00000418169.1:n.*25G>A
NM_003179.2:c.*4+21G>A	NP_003170.1:n.*4+21G>A
XM_011543950.1:c.*4+21G>A	XP_011542252.1:n.*4+21G>A
XM_011543951.1:c.*4+21G>A	XP_011542253.1:n.*4+21G>A
NM_003179.3:c.*4+21G>A MANE Select	NP_003170.1:n.*4+21G>A