Canonical Allele Identifier: CA645604068

Gene: STK11

Linked Data

• COSMIC: COSM51203

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220375_1221342del , CM000681.2:g.1220375_1221342del	GRCh38
NC_000019.9:g.1220374_1221341del , CM000681.1:g.1220374_1221341del	GRCh37
NC_000019.8:g.1171374_1172341del	NCBI36
NG_007460.2:g.35969_36936del , LRG_319:g.35969_36936del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.467_862+2del
ENST00000585748.3:c.95_490+2del
ENST00000585851.2:c.293_688+2del
ENST00000326873.12:c.467_862+2del
ENST00000652231.1:c.467_862+2del
ENST00000326873.11:c.467_862+2del
ENST00000586243.5:c.467_862+2del
ENST00000586358.5:n.290_760+2del
ENST00000589152.5:n.557_954del
ENST00000591133.2:n.363_833+2del
NM_000455.4:c.467_862+2del , LRG_319t1:c.467_862+2del
XM_005259617.1:c.467_862+2del
XM_005259618.3:c.467_862+2del
XM_011528209.1:c.245_640+2del
XR_936204.1:n.1092_1487+2del
XM_005259617.3:c.467_862+2del
XM_011528209.2:c.245_640+2del
XR_001753738.2:n.1092_1487+2del
XR_001753739.1:n.1092_1487+2del
XR_001753740.2:n.1092_1487+2del
NM_000455.5:c.467_862+2del