Canonical Allele Identifier: CA2582597430

Gene: STK11

Linked Data

• gnomAD v4: 19-1226518-TATG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226520_1226522del , CM000681.2:g.1226520_1226522del	GRCh38
NC_000019.9:g.1226519_1226521del , CM000681.1:g.1226519_1226521del	GRCh37
NC_000019.8:g.1177519_1177521del	NCBI36
NG_007460.2:g.42114_42116del , LRG_319:g.42114_42116del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2776_*2778del	ENSP00000490268.2:n.*2776_*2778del
ENST00000585748.3:c.803_805del	ENSP00000477641.2:p.Met268del
ENST00000585851.2:c.1001_1003del	ENSP00000467912.2:p.Met334del
ENST00000326873.12:c.1175_1177del MANE Select	ENSP00000324856.6:p.Met392del
ENST00000326873.11:c.1175_1177del	ENSP00000324856.6:p.Met392del
ENST00000585465.2:n.2908_2910del
ENST00000586243.5:c.1175_1177del	ENSP00000467240.2:p.Met392del
ENST00000589152.5:n.1873_1875del
NM_000455.4:c.1175_1177del , LRG_319t1:c.1175_1177del	NP_000446.1:p.Met392del
XM_005259617.1:c.1170_1172del	XP_005259674.1:p.Tyr390Ter
XM_011528209.1:c.948_950del	XP_011526511.1:p.Tyr316Ter
XM_005259617.3:c.1170_1172del	XP_005259674.1:p.Tyr390Ter
XM_011528209.2:c.948_950del	XP_011526511.1:p.Tyr316Ter
XR_001753738.2:n.1981_1983del
XR_001753740.2:n.1951_1953del
NM_000455.5:c.1175_1177del MANE Select	NP_000446.1:p.Met392del