Canonical Allele Identifier: CA11953152
Gene: STK10 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17570583

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172132527G>A , CM000667.2:g.172132527G>A GRCh38
NC_000005.9:g.171559531G>A , CM000667.1:g.171559531G>A GRCh37
NC_000005.8:g.171492136G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_005990.3:c.322-5106C>T VV NP_005981.3:p.=
XM_011534641.1:c.322-5106C>T XP_011532943.1:p.=
XM_011534643.1:c.322-5106C>T XP_011532945.1:p.=
XM_011534644.1:c.322-5106C>T XP_011532946.1:p.=
XM_017009788.1:c.-3-5106C>T XP_016865277.1:p.=
NM_005990.4:c.322-5106C>T VV MANE Preferred NP_005981.3:p.=
ENST00000176763.9:c.322-5106C>T ENSP00000176763.5:p.=
ENST00000519710.1:n.103-5106C>T