Canonical Allele Identifier: CA2428531453
Gene: SYP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49191420G= , CM000685.2:g.49191420G= GRCh38
NC_000023.10:g.49047877G= , CM000685.1:g.49047877G= GRCh37
NC_000023.9:g.48934821G= NCBI36
NG_012532.1:g.13785C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689634.1:n.2546C=
ENST00000692723.1:n.972+13C=
ENST00000263233.9:c.*4+13C= MANE Select ENSP00000263233.4:n.*4+13C=
ENST00000263233.8:c.*4+13C= ENSP00000263233.4:n.*4+13C=
ENST00000376303.6:c.*698+13C= ENSP00000365480.2:n.*698+13C=
ENST00000472598.5:c.615+13C=
ENST00000479808.5:c.*17C= ENSP00000418169.1:n.*17C=
NM_003179.2:c.*4+13C= NP_003170.1:n.*4+13C=
XM_011543950.1:c.*4+13C= XP_011542252.1:n.*4+13C=
XM_011543951.1:c.*4+13C= XP_011542253.1:n.*4+13C=
NM_003179.3:c.*4+13C= MANE Select NP_003170.1:n.*4+13C=