Canonical Allele Identifier: CA1601147038
Gene: STK10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172132480G= , CM000667.2:g.172132480G= GRCh38
NC_000005.9:g.171559484G= , CM000667.1:g.171559484G= GRCh37
NC_000005.8:g.171492089G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000176763.10:c.322-5059C= MANE Select ENSP00000176763.5:n.322-5059C=
ENST00000176763.9:c.322-5059C= ENSP00000176763.5:n.322-5059C=
ENST00000519710.1:n.103-5059C=
NM_005990.3:c.322-5059C= NP_005981.3:n.322-5059C=
XM_011534641.1:c.322-5059C= XP_011532943.1:n.322-5059C=
XM_011534643.1:c.322-5059C= XP_011532945.1:n.322-5059C=
XM_011534644.1:c.322-5059C= XP_011532946.1:n.322-5059C=
XM_017009788.1:c.-3-5059C= XP_016865277.1:n.-3-5059C=
NM_005990.4:c.322-5059C= MANE Select NP_005981.3:n.322-5059C=