Canonical Allele Identifier: CA504708554

Gene: STK11

Linked Data

• dbSNP Id: rs201256614
• gnomAD v4: 19-1226623-G-C
• MyVariant Identifiers: chr19:g.1226622G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226623G>C , CM000681.2:g.1226623G>C	GRCh38
NC_000019.9:g.1226622G>C , CM000681.1:g.1226622G>C	GRCh37
NC_000019.8:g.1177622G>C	NCBI36
NG_007460.2:g.42217G>C , LRG_319:g.42217G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2879G>C	ENSP00000490268.2:n.*2879G>C
ENST00000585748.3:c.906G>C	ENSP00000477641.2:p.Arg302=
ENST00000585851.2:c.1104G>C	ENSP00000467912.2:p.Arg368=
ENST00000326873.12:c.1278G>C MANE Select	ENSP00000324856.6:p.Arg426=
ENST00000326873.11:c.1278G>C	ENSP00000324856.6:p.Arg426=
ENST00000585465.2:n.3011G>C
ENST00000586243.5:c.1275G>C	ENSP00000467240.2:p.Arg425=
ENST00000589152.5:n.1976G>C
NM_000455.4:c.1278G>C , LRG_319t1:c.1278G>C	NP_000446.1:p.Arg426=
XM_005259617.1:c.1273G>C	XP_005259674.1:p.Ala425Pro
XM_011528209.1:c.1051G>C	XP_011526511.1:p.Ala351Pro
XM_005259617.3:c.1273G>C	XP_005259674.1:p.Ala425Pro
XM_011528209.2:c.1051G>C	XP_011526511.1:p.Ala351Pro
XR_001753738.2:n.2084G>C
XR_001753740.2:n.2054G>C
NM_000455.5:c.1278G>C MANE Select	NP_000446.1:p.Arg426=