Canonical Allele Identifier: CA2016045558
Gene: STYK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.10653686T>A , CM000674.2:g.10653686T>A GRCh38
NC_000012.11:g.10806285T>A , CM000674.1:g.10806285T>A GRCh37
NC_000012.10:g.10697552T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000075503.8:c.-194-16490A>T MANE Select ENSP00000075503.3:n.-194-16490A>T
ENST00000075503.7:c.-194-16490A>T ENSP00000075503.3:n.-194-16490A>T
ENST00000535345.5:c.-259-12952A>T ENSP00000444488.1:n.-259-12952A>T
ENST00000538867.5:c.-194-16490A>T ENSP00000445391.1:n.-194-16490A>T
ENST00000541561.1:c.-68-19000A>T ENSP00000444942.1:n.-68-19000A>T
ENST00000542562.5:c.-69+13603A>T ENSP00000446241.1:n.-69+13603A>T
NM_018423.2:c.-194-16490A>T NP_060893.2:n.-194-16490A>T
XM_005253417.2:c.-68-19000A>T XP_005253474.1:n.-68-19000A>T
XM_011520736.1:c.-259-12952A>T XP_011519038.1:n.-259-12952A>T
XM_011520737.1:c.-195+13603A>T XP_011519039.1:n.-195+13603A>T
XM_011520738.1:c.-194-16490A>T XP_011519040.1:n.-194-16490A>T
XM_011520739.1:c.-194-16490A>T XP_011519041.1:n.-194-16490A>T
XM_011520737.2:c.-195+13603A>T XP_011519039.1:n.-195+13603A>T
XM_011520738.2:c.-194-16490A>T XP_011519040.1:n.-194-16490A>T
XM_017019579.1:c.-565-16490A>T XP_016875068.1:n.-565-16490A>T
NM_018423.3:c.-194-16490A>T MANE Select NP_060893.2:n.-194-16490A>T