Canonical Allele Identifier: CA2581564229

Gene: STK19

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31973120A>C , CM000668.2:g.31973120A>C	GRCh38
NC_000006.11:g.31940897A>C , CM000668.1:g.31940897A>C	GRCh37
NC_000006.10:g.32048876A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000685781.1:c.237+363A>C MANE Select	ENSP00000509445.1:n.237+363A>C
ENST00000375331.7:c.237+363A>C	ENSP00000364480.3:n.237+363A>C
ENST00000375333.3:c.237+363A>C	ENSP00000364482.3:n.237+363A>C
ENST00000483801.6:c.100+609A>C	ENSP00000418866.2:n.100+609A>C
ENST00000519179.6:c.100+609A>C	ENSP00000454870.2:n.100+609A>C
ENST00000375331.6:c.567+363A>C	ENSP00000364480.2:n.567+363A>C
ENST00000375333.2:c.567+363A>C	ENSP00000364482.2:n.567+363A>C
ENST00000463823.5:n.138+609A>C
ENST00000466132.5:n.964+363A>C
ENST00000466336.5:n.252+363A>C
ENST00000469907.1:n.338+201A>C
ENST00000471028.1:n.223+363A>C
ENST00000473983.5:n.309+363A>C
ENST00000478486.5:n.459+201A>C
ENST00000479644.1:n.1096A>C
ENST00000483801.5:c.131+609A>C
ENST00000484540.5:n.180+363A>C
ENST00000491861.5:n.203+363A>C
ENST00000492583.5:n.750+363A>C
ENST00000519179.5:c.131+609A>C
NM_004197.1:c.567+363A>C	NP_004188.1:n.567+363A>C
NM_032454.1:c.567+363A>C	NP_115830.1:n.567+363A>C
NR_026717.1:n.880+363A>C
NM_004197.2:c.237+363A>C MANE Select	NP_004188.2:n.237+363A>C