Canonical Allele Identifier: CA2579606723

Gene: SYP

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49191403_49191405del , CM000685.2:g.49191403_49191405del	GRCh38
NC_000023.10:g.49047860_49047862del , CM000685.1:g.49047860_49047862del	GRCh37
NC_000023.9:g.48934804_48934806del	NCBI36
NG_012532.1:g.13803_13805del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689634.1:n.2564_2566del
ENST00000692723.1:n.972+31_972+33del
ENST00000263233.9:c.*4+31_*4+33del MANE Select	ENSP00000263233.4:n.*4+31_*4+33del
ENST00000263233.8:c.*4+31_*4+33del	ENSP00000263233.4:n.*4+31_*4+33del
ENST00000376303.6:c.*698+31_*698+33del	ENSP00000365480.2:n.*698+31_*698+33del
ENST00000472598.5:c.615+31_615+33del
ENST00000479808.5:c.*35_*37del	ENSP00000418169.1:n.*35_*37del
NM_003179.2:c.*4+31_*4+33del	NP_003170.1:n.*4+31_*4+33del
XM_011543950.1:c.*4+31_*4+33del	XP_011542252.1:n.*4+31_*4+33del
XM_011543951.1:c.*4+31_*4+33del	XP_011542253.1:n.*4+31_*4+33del
NM_003179.3:c.*4+31_*4+33del MANE Select	NP_003170.1:n.*4+31_*4+33del