Canonical Allele Identifier: CA3265808145

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218335_1218467del , CM000681.2:g.1218335_1218467del	GRCh38
NC_000019.9:g.1218334_1218466del , CM000681.1:g.1218334_1218466del	GRCh37
NC_000019.8:g.1169334_1169466del	NCBI36
NG_007460.2:g.33929_34061del , LRG_319:g.33929_34061del

Transcript Alleles

HGVS	Amino-acid Change
NM_000455.4:c.291-82_341del , LRG_319t1:c.291-82_341del
NM_000455.5:c.291-82_341del
ENST00000326873.11:c.291-82_341del
ENST00000326873.12:c.291-82_341del
ENST00000585465.3:c.291-82_341del
ENST00000585748.2:c.-82-82_-32del
ENST00000585748.3:c.-82-82_-32del
ENST00000585851.1:c.291-2038_291-1906del	ENSP00000467912.1:n.291-2038_291-1906del
ENST00000585851.2:c.291-2038_291-1906del	ENSP00000467912.2:n.291-2038_291-1906del
ENST00000586243.5:c.291-82_341del
ENST00000586358.5:n.114-82_164del
ENST00000589152.5:n.381-82_431del
ENST00000593219.5:c.*116-82_*166del
ENST00000652231.1:c.291-82_341del
XM_005259617.1:c.291-82_341del
XM_005259617.3:c.291-82_341del
XM_005259618.3:c.291-82_341del
XM_011528209.1:c.69-82_119del
XM_011528209.2:c.69-82_119del
XR_001753738.2:n.916-82_966del
XR_001753739.1:n.916-82_966del
XR_001753740.2:n.916-82_966del
XR_936204.1:n.916-82_966del