Canonical Allele Identifier: CA136920446

Gene: STK19

Linked Data

• dbSNP Id: rs934034679
• gnomAD v4: 6-31973123-G-A
• MyVariant Identifiers: chr6:g.31940900G>A (hg19) ; chr6:g.31973123G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31973123G>A , CM000668.2:g.31973123G>A	GRCh38
NC_000006.11:g.31940900G>A , CM000668.1:g.31940900G>A	GRCh37
NC_000006.10:g.32048879G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000685781.1:c.237+366G>A MANE Select	ENSP00000509445.1:n.237+366G>A
ENST00000375331.7:c.237+366G>A	ENSP00000364480.3:n.237+366G>A
ENST00000375333.3:c.237+366G>A	ENSP00000364482.3:n.237+366G>A
ENST00000483801.6:c.100+612G>A	ENSP00000418866.2:n.100+612G>A
ENST00000519179.6:c.100+612G>A	ENSP00000454870.2:n.100+612G>A
ENST00000375331.6:c.567+366G>A	ENSP00000364480.2:n.567+366G>A
ENST00000375333.2:c.567+366G>A	ENSP00000364482.2:n.567+366G>A
ENST00000463823.5:n.138+612G>A
ENST00000466132.5:n.964+366G>A
ENST00000466336.5:n.252+366G>A
ENST00000469907.1:n.338+204G>A
ENST00000471028.1:n.223+366G>A
ENST00000473983.5:n.309+366G>A
ENST00000478486.5:n.459+204G>A
ENST00000479644.1:n.1099G>A
ENST00000483801.5:c.131+612G>A
ENST00000484540.5:n.180+366G>A
ENST00000491861.5:n.203+366G>A
ENST00000492583.5:n.750+366G>A
ENST00000519179.5:c.131+612G>A
NM_004197.1:c.567+366G>A	NP_004188.1:n.567+366G>A
NM_032454.1:c.567+366G>A	NP_115830.1:n.567+366G>A
NR_026717.1:n.880+366G>A
NM_004197.2:c.237+366G>A MANE Select	NP_004188.2:n.237+366G>A