Canonical Allele Identifier: CA2366012752

Gene: STK4

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44975362C>A , CM000682.2:g.44975362C>A	GRCh38
NC_000020.10:g.43604003C>A , CM000682.1:g.43604003C>A	GRCh37
NC_000020.9:g.43037417C>A	NCBI36
NG_032172.1:g.13884C>A , LRG_535:g.13884C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474717.3:c.-112-3081C>A	ENSP00000479564.2:n.-112-3081C>A
ENST00000487587.3:c.*1317C>A	ENSP00000482076.1:n.*1317C>A
ENST00000488618.2:n.2710C>A
ENST00000499879.7:c.117-3081C>A	ENSP00000443514.1:n.117-3081C>A
ENST00000698219.1:c.*1439C>A	ENSP00000513612.1:n.*1439C>A
ENST00000698220.1:c.*1342C>A	ENSP00000513613.1:n.*1342C>A
ENST00000698221.1:c.117-3081C>A	ENSP00000513614.1:n.117-3081C>A
ENST00000698222.1:c.*29C>A	ENSP00000513615.1:n.*29C>A
ENST00000698223.1:n.231-3081C>A
ENST00000698224.1:c.22-3081C>A
ENST00000372806.8:c.117-3081C>A MANE Select	ENSP00000361892.3:n.117-3081C>A
ENST00000372801.5:c.117-3081C>A	ENSP00000361887.1:n.117-3081C>A
ENST00000372806.7:c.117-3081C>A	ENSP00000361892.3:n.117-3081C>A
ENST00000474717.2:c.-112-3081C>A	ENSP00000479564.1:n.-112-3081C>A
ENST00000487587.2:c.*1317C>A	ENSP00000482076.1:n.*1317C>A
ENST00000499879.6:c.117-3081C>A	ENSP00000443514.1:n.117-3081C>A
NM_006282.2:c.117-3081C>A , LRG_535t1:c.117-3081C>A	NP_006273.1:n.117-3081C>A
XM_005260530.2:c.165-3081C>A	XP_005260587.1:n.165-3081C>A
XM_005260531.2:c.165-3081C>A	XP_005260588.1:n.165-3081C>A
XM_005260532.2:c.29C>A	XP_005260589.1:p.Thr10Asn
XM_005260533.2:c.117-3081C>A	XP_005260590.1:n.117-3081C>A
XM_011529018.1:c.-113+1929C>A	XP_011527320.1:n.-113+1929C>A
XM_011529019.1:c.-113+1929C>A	XP_011527321.1:n.-113+1929C>A
XM_011529020.1:c.165-3081C>A	XP_011527322.1:n.165-3081C>A
NM_001352385.1:c.117-3081C>A	NP_001339314.1:n.117-3081C>A
NM_006282.4:c.117-3081C>A	NP_006273.1:n.117-3081C>A
NR_147974.1:n.1611C>A
XM_005260531.3:c.165-3081C>A	XP_005260588.1:n.165-3081C>A
XM_005260532.4:c.29C>A	XP_005260589.1:p.Thr10Asn
XM_011529018.3:c.-113+1929C>A	XP_011527320.1:n.-113+1929C>A
XM_011529020.2:c.165-3081C>A	XP_011527322.1:n.165-3081C>A
XM_017028029.2:c.29C>A	XP_016883518.1:p.Thr10Asn
XM_017028030.2:c.29C>A	XP_016883519.1:p.Thr10Asn
XM_017028031.2:c.29C>A	XP_016883520.1:p.Thr10Asn
XM_017028032.2:c.-51C>A	XP_016883521.1:n.-51C>A
XM_017028033.2:c.117-3081C>A	XP_016883522.1:n.117-3081C>A
NM_006282.5:c.117-3081C>A MANE Select	NP_006273.1:n.117-3081C>A
NM_001352385.2:c.117-3081C>A	NP_001339314.1:n.117-3081C>A
NR_147974.2:n.1569C>A