Canonical Allele Identifier: CA875955155
Gene: SYP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49191418T>C , CM000685.2:g.49191418T>C GRCh38
NC_000023.10:g.49047875T>C , CM000685.1:g.49047875T>C GRCh37
NC_000023.9:g.48934819T>C NCBI36
NG_012532.1:g.13787A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689634.1:n.2548A>G
ENST00000692723.1:n.972+15A>G
ENST00000263233.9:c.*4+15A>G MANE Select ENSP00000263233.4:n.*4+15A>G
ENST00000263233.8:c.*4+15A>G ENSP00000263233.4:n.*4+15A>G
ENST00000376303.6:c.*698+15A>G ENSP00000365480.2:n.*698+15A>G
ENST00000472598.5:c.615+15A>G
ENST00000479808.5:c.*19A>G ENSP00000418169.1:n.*19A>G
NM_003179.2:c.*4+15A>G NP_003170.1:n.*4+15A>G
XM_011543950.1:c.*4+15A>G XP_011542252.1:n.*4+15A>G
XM_011543951.1:c.*4+15A>G XP_011542253.1:n.*4+15A>G
NM_003179.3:c.*4+15A>G MANE Select NP_003170.1:n.*4+15A>G