Canonical Allele Identifier: CA394112277

Gene: STUB1 MSLN

Linked Data

• MyVariant Identifiers: chr16:g.731521A>G (hg19) ; chr16:g.681521A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681521A>G , CM000678.2:g.681521A>G	GRCh38
NC_000016.9:g.731521A>G , CM000678.1:g.731521A>G	GRCh37
NC_000016.8:g.671522A>G	NCBI36
NG_034141.1:g.6411A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.442A>G (STUB1) MANE Select	ENSP00000219548.4:p.Asn148Asp
ENST00000219548.8:c.442A>G (STUB1)	ENSP00000219548.4:p.Asn148Asp
ENST00000563505.5:n.538A>G (STUB1)
ENST00000564316.1:c.41A>G (STUB1)
ENST00000564370.5:c.226A>G (STUB1)	ENSP00000456875.1:p.Asn76Asp
ENST00000565677.5:c.226A>G (STUB1)	ENSP00000457228.1:p.Asn76Asp
ENST00000566181.2:n.211A>G (STUB1)
ENST00000566408.5:c.159A>G (STUB1)
ENST00000567173.5:c.385A>G (STUB1)	ENSP00000456591.1:p.Asn129Asp
ENST00000569248.5:n.1016A>G (STUB1)
ENST00000620831.4:c.-50+38218A>G (MSLN)	ENSP00000482893.1:n.-50+38218A>G
NM_001293197.1:c.226A>G (STUB1)	NP_001280126.1:p.Asn76Asp
NM_005861.3:c.442A>G (STUB1)	NP_005852.2:p.Asn148Asp
NM_005861.4:c.442A>G (STUB1) MANE Select	NP_005852.2:p.Asn148Asp
NM_001293197.2:c.226A>G (STUB1)	NP_001280126.1:p.Asn76Asp