Canonical Allele Identifier: CA2428531421

Gene: SYP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49191341_49191342delinsCG , CM000685.2:g.49191341_49191342delinsCG	GRCh38
NC_000023.10:g.49047798_49047799delinsCG , CM000685.1:g.49047798_49047799delinsCG	GRCh37
NC_000023.9:g.48934742_48934743delinsCG	NCBI36
NG_012532.1:g.13863_13864delinsCG

Transcript Alleles

HGVS	Amino-acid Change
NM_003179.3:c.*4+91_*4+92delinsCG MANE Select	NP_003170.1:n.*4+91_*4+92delinsCG
ENST00000263233.9:c.*4+91_*4+92delinsCG MANE Select	ENSP00000263233.4:n.*4+91_*4+92delinsCG
NM_003179.2:c.*4+91_*4+92delinsCG	NP_003170.1:n.*4+91_*4+92delinsCG
ENST00000263233.8:c.*4+91_*4+92delinsCG	ENSP00000263233.4:n.*4+91_*4+92delinsCG
ENST00000376303.6:c.*698+91_*698+92delinsCG	ENSP00000365480.2:n.*698+91_*698+92delinsCG
ENST00000472598.5:c.615+91_615+92delinsCG
ENST00000479808.5:c.*95_*96delinsCG	ENSP00000418169.1:n.*95_*96delinsCG
ENST00000689634.1:n.2624_2625delinsCG
ENST00000692723.1:n.972+91_972+92delinsCG
XM_011543950.1:c.*4+91_*4+92delinsCG	XP_011542252.1:n.*4+91_*4+92delinsCG
XM_011543951.1:c.*4+91_*4+92delinsCG	XP_011542253.1:n.*4+91_*4+92delinsCG