Canonical Allele Identifier: CA2201204658

Gene: STUB1 MSLN

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.681620A= , CM000678.2:g.681620A=	GRCh38
NC_000016.9:g.731620A= , CM000678.1:g.731620A=	GRCh37
NC_000016.8:g.671621A=	NCBI36
NG_034141.1:g.6510A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000219548.9:c.524+17A= (STUB1) MANE Select	ENSP00000219548.4:n.524+17A=
ENST00000219548.8:c.524+17A= (STUB1)	ENSP00000219548.4:n.524+17A=
ENST00000563505.5:n.620+17A= (STUB1)
ENST00000564316.1:c.123+17A= (STUB1)
ENST00000564370.5:c.308+17A= (STUB1)	ENSP00000456875.1:n.308+17A=
ENST00000565677.5:c.308+17A= (STUB1)	ENSP00000457228.1:n.308+17A=
ENST00000566181.2:n.293+17A= (STUB1)
ENST00000566408.5:c.241+17A= (STUB1)
ENST00000567173.5:c.467+17A= (STUB1)	ENSP00000456591.1:n.467+17A=
ENST00000569248.5:n.1098+17A= (STUB1)
ENST00000620831.4:c.-50+38317A= (MSLN)	ENSP00000482893.1:n.-50+38317A=
NM_001293197.1:c.308+17A= (STUB1)	NP_001280126.1:n.308+17A=
NM_005861.3:c.524+17A= (STUB1)	NP_005852.2:n.524+17A=
NM_005861.4:c.524+17A= (STUB1) MANE Select	NP_005852.2:n.524+17A=
NM_001293197.2:c.308+17A= (STUB1)	NP_001280126.1:n.308+17A=