Canonical Allele Identifier: CA394112419

Gene: STUB1 MSLN

Linked Data

• dbSNP Id: rs1396282737
• gnomAD v2: 16-731547-C-G
• gnomAD v4: 16-681547-C-G
• MyVariant Identifiers: chr16:g.731547C>G (hg19) ; chr16:g.681547C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681547C>G , CM000678.2:g.681547C>G	GRCh38
NC_000016.9:g.731547C>G , CM000678.1:g.731547C>G	GRCh37
NC_000016.8:g.671548C>G	NCBI36
NG_034141.1:g.6437C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.468C>G (STUB1) MANE Select	ENSP00000219548.4:p.His156Gln
ENST00000219548.8:c.468C>G (STUB1)	ENSP00000219548.4:p.His156Gln
ENST00000563505.5:n.564C>G (STUB1)
ENST00000564316.1:c.67C>G (STUB1)
ENST00000564370.5:c.252C>G (STUB1)	ENSP00000456875.1:p.His84Gln
ENST00000565677.5:c.252C>G (STUB1)	ENSP00000457228.1:p.His84Gln
ENST00000566181.2:n.237C>G (STUB1)
ENST00000566408.5:c.185C>G (STUB1)
ENST00000567173.5:c.411C>G (STUB1)	ENSP00000456591.1:p.His137Gln
ENST00000569248.5:n.1042C>G (STUB1)
ENST00000620831.4:c.-50+38244C>G (MSLN)	ENSP00000482893.1:n.-50+38244C>G
NM_001293197.1:c.252C>G (STUB1)	NP_001280126.1:p.His84Gln
NM_005861.3:c.468C>G (STUB1)	NP_005852.2:p.His156Gln
NM_005861.4:c.468C>G (STUB1) MANE Select	NP_005852.2:p.His156Gln
NM_001293197.2:c.252C>G (STUB1)	NP_001280126.1:p.His84Gln