Canonical Allele Identifier: CA2678079449

Gene: STK19

Linked Data

• gnomAD v4: 6-31973127-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31973128del , CM000668.2:g.31973128del	GRCh38
NC_000006.11:g.31940905del , CM000668.1:g.31940905del	GRCh37
NC_000006.10:g.32048884del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000685781.1:c.237+371del MANE Select	ENSP00000509445.1:n.237+371del
ENST00000375331.7:c.237+371del	ENSP00000364480.3:n.237+371del
ENST00000375333.3:c.237+371del	ENSP00000364482.3:n.237+371del
ENST00000483801.6:c.100+617del	ENSP00000418866.2:n.100+617del
ENST00000519179.6:c.100+617del	ENSP00000454870.2:n.100+617del
ENST00000375331.6:c.567+371del	ENSP00000364480.2:n.567+371del
ENST00000375333.2:c.567+371del	ENSP00000364482.2:n.567+371del
ENST00000463823.5:n.138+617del
ENST00000466132.5:n.964+371del
ENST00000466336.5:n.252+371del
ENST00000469907.1:n.338+209del
ENST00000471028.1:n.223+371del
ENST00000473983.5:n.309+371del
ENST00000478486.5:n.459+209del
ENST00000479644.1:n.1104del
ENST00000483801.5:c.131+617del
ENST00000484540.5:n.180+371del
ENST00000491861.5:n.203+371del
ENST00000492583.5:n.750+371del
ENST00000519179.5:c.131+617del
NM_004197.1:c.567+371del	NP_004188.1:n.567+371del
NM_032454.1:c.567+371del	NP_115830.1:n.567+371del
NR_026717.1:n.880+371del
NM_004197.2:c.237+371del MANE Select	NP_004188.2:n.237+371del