Canonical Allele Identifier: CA394112158

Gene: STUB1 MSLN

Linked Data

• gnomAD v4: 16-681502-C-G
• MyVariant Identifiers: chr16:g.731502C>G (hg19) ; chr16:g.681502C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681502C>G , CM000678.2:g.681502C>G	GRCh38
NC_000016.9:g.731502C>G , CM000678.1:g.731502C>G	GRCh37
NC_000016.8:g.671503C>G	NCBI36
NG_034141.1:g.6392C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.423C>G (STUB1) MANE Select	ENSP00000219548.4:p.Ile141Met
ENST00000219548.8:c.423C>G (STUB1)	ENSP00000219548.4:p.Ile141Met
ENST00000563505.5:n.519C>G (STUB1)
ENST00000564316.1:c.22C>G (STUB1)
ENST00000564370.5:c.207C>G (STUB1)	ENSP00000456875.1:p.Ile69Met
ENST00000565677.5:c.207C>G (STUB1)	ENSP00000457228.1:p.Ile69Met
ENST00000566181.2:n.192C>G (STUB1)
ENST00000566408.5:c.140C>G (STUB1)
ENST00000567173.5:c.366C>G (STUB1)	ENSP00000456591.1:p.Ile122Met
ENST00000569248.5:n.997C>G (STUB1)
ENST00000620831.4:c.-50+38199C>G (MSLN)	ENSP00000482893.1:n.-50+38199C>G
NM_001293197.1:c.207C>G (STUB1)	NP_001280126.1:p.Ile69Met
NM_005861.3:c.423C>G (STUB1)	NP_005852.2:p.Ile141Met
NM_005861.4:c.423C>G (STUB1) MANE Select	NP_005852.2:p.Ile141Met
NM_001293197.2:c.207C>G (STUB1)	NP_001280126.1:p.Ile69Met