Canonical Allele Identifier: CA409124201
Community Standard Title: NM_006282.5(STK4):c.395C>G (p.Ser132Ter)
Gene: STK4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44987166C>G , CM000682.2:g.44987166C>G GRCh38
NC_000020.10:g.43615807C>G , CM000682.1:g.43615807C>G GRCh37
NC_000020.9:g.43049221C>G NCBI36
NG_032172.1:g.25688C>G , LRG_535:g.25688C>G

Transcript Alleles

HGVS Amino-acid Change
NM_006282.5:c.395C>G MANE Select NP_006273.1:p.Ser132Ter
ENST00000372806.8:c.395C>G MANE Select ENSP00000361892.3:p.Ser132Ter
NM_001352385.1:c.395C>G NP_001339314.1:p.Ser132Ter
NM_001352385.2:c.395C>G NP_001339314.1:p.Ser132Ter
NM_006282.2:c.395C>G , LRG_535t1:c.395C>G NP_006273.1:p.Ser132Ter
NM_006282.4:c.395C>G NP_006273.1:p.Ser132Ter
ENST00000372801.5:c.395C>G ENSP00000361887.1:p.Ser132Ter
ENST00000372806.7:c.395C>G ENSP00000361892.3:p.Ser132Ter
ENST00000474717.2:c.167C>G ENSP00000479564.1:p.Ser56Ter
ENST00000474717.3:c.167C>G ENSP00000479564.2:p.Ser56Ter
ENST00000499879.6:c.360+5223C>G ENSP00000443514.1:n.360+5223C>G
ENST00000499879.7:c.360+5223C>G ENSP00000443514.1:n.360+5223C>G
ENST00000698221.1:c.395C>G ENSP00000513614.1:p.Ser132Ter
ENST00000698222.1:c.*356C>G ENSP00000513615.1:n.*356C>G
ENST00000698224.1:c.293C>G
ENST00000698225.1:n.595C>G
ENST00000698226.1:n.182C>G
ENST00000698227.1:n.33C>G
XM_005260530.2:c.443C>G XP_005260587.1:p.Ser148Ter
XM_005260531.2:c.443C>G XP_005260588.1:p.Ser148Ter
XM_005260531.3:c.443C>G XP_005260588.1:p.Ser148Ter
XM_005260532.2:c.356C>G XP_005260589.1:p.Ser119Ter
XM_005260532.4:c.356C>G XP_005260589.1:p.Ser119Ter
XM_005260533.2:c.395C>G XP_005260590.1:p.Ser132Ter
XM_011529017.1:c.308C>G XP_011527319.1:p.Ser103Ter
XM_011529018.1:c.167C>G XP_011527320.1:p.Ser56Ter
XM_011529018.3:c.167C>G XP_011527320.1:p.Ser56Ter
XM_011529019.1:c.167C>G XP_011527321.1:p.Ser56Ter
XM_011529020.1:c.443C>G XP_011527322.1:p.Ser148Ter
XM_011529020.2:c.443C>G XP_011527322.1:p.Ser148Ter
XM_017028029.2:c.356C>G XP_016883518.1:p.Ser119Ter
XM_017028030.2:c.356C>G XP_016883519.1:p.Ser119Ter
XM_017028031.2:c.356C>G XP_016883520.1:p.Ser119Ter
XM_017028032.2:c.308C>G XP_016883521.1:p.Ser103Ter
XM_017028033.2:c.395C>G XP_016883522.1:p.Ser132Ter