Canonical Allele Identifier: CA13642497

Gene: STYK1

Genomic Alleles

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

Transcript Alleles

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