Canonical Allele Identifier: CA394111896

Gene: STUB1 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.731443A>C (hg19) ; chr16:g.681443A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681443A>C , CM000678.2:g.681443A>C	GRCh38
NC_000016.9:g.731443A>C , CM000678.1:g.731443A>C	GRCh37
NC_000016.8:g.671444A>C	NCBI36
NG_034141.1:g.6333A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.364A>C (STUB1) MANE Select	ENSP00000219548.4:p.Ser122Arg
ENST00000219548.8:c.364A>C (STUB1)	ENSP00000219548.4:p.Ser122Arg
ENST00000563505.5:n.460A>C (STUB1)
ENST00000564370.5:c.148A>C (STUB1)	ENSP00000456875.1:p.Ser50Arg
ENST00000565677.5:c.148A>C (STUB1)	ENSP00000457228.1:p.Ser50Arg
ENST00000566181.2:n.133A>C (STUB1)
ENST00000566408.5:c.81A>C (STUB1)
ENST00000567173.5:c.307A>C (STUB1)	ENSP00000456591.1:p.Ser103Arg
ENST00000569248.5:n.938A>C (STUB1)
ENST00000620831.4:c.-50+38140A>C (MSLN)	ENSP00000482893.1:n.-50+38140A>C
NM_001293197.1:c.148A>C (STUB1)	NP_001280126.1:p.Ser50Arg
NM_005861.3:c.364A>C (STUB1)	NP_005852.2:p.Ser122Arg
NM_005861.4:c.364A>C (STUB1) MANE Select	NP_005852.2:p.Ser122Arg
NM_001293197.2:c.148A>C (STUB1)	NP_001280126.1:p.Ser50Arg