Canonical Allele Identifier: CA13850759
Gene: STK24 HGNC NCBI

Linked Data

dbSNP Id: rs9517320

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.98474049A>C , CM000675.2:g.98474049A>C GRCh38
NC_000013.10:g.99126303A>C , CM000675.1:g.99126303A>C GRCh37
NC_000013.9:g.97924304A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000539966.6:c.597+772T>G MANE Select ENSP00000442539.2:n.597+772T>G
ENST00000376547.7:c.633+772T>G ENSP00000365730.3:n.633+772T>G
ENST00000397517.6:c.540+772T>G ENSP00000380651.3:n.540+772T>G
ENST00000444574.1:c.349+772T>G
ENST00000539966.5:c.597+772T>G ENSP00000442539.2:n.597+772T>G
NM_001032296.3:c.597+772T>G NP_001027467.2:n.597+772T>G
NM_001286649.1:c.540+772T>G NP_001273578.1:n.540+772T>G
NM_003576.4:c.633+772T>G NP_003567.2:n.633+772T>G
XM_005254078.3:c.303+772T>G XP_005254135.1:n.303+772T>G
XM_005254079.3:c.303+772T>G XP_005254136.1:n.303+772T>G
XM_005254079.5:c.303+772T>G XP_005254136.1:n.303+772T>G
XM_017020794.2:c.855+772T>G XP_016876283.1:n.855+772T>G
XM_024449426.1:c.303+772T>G XP_024305194.1:n.303+772T>G
NM_001032296.4:c.597+772T>G MANE Select NP_001027467.2:n.597+772T>G
NM_001286649.2:c.540+772T>G NP_001273578.1:n.540+772T>G
NM_003576.5:c.633+772T>G NP_003567.2:n.633+772T>G