Canonical Allele Identifier: CA1874916101

Gene: ASTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.116782154T= , CM000671.2:g.116782154T=	GRCh38
NC_000009.11:g.119544433T= , CM000671.1:g.119544433T=	GRCh37
NC_000009.10:g.118584254T=	NCBI36
NG_021409.1:g.637885A=
NG_021409.2:g.637904A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313400.9:c.2396+23478A= MANE Select	ENSP00000314038.4:n.2396+23478A=
ENST00000361477.8:c.2243+23478A=	ENSP00000355116.5:n.2243+23478A=
ENST00000313400.8:c.2396+23478A=	ENSP00000314038.4:n.2396+23478A=
ENST00000361209.6:c.2243+23478A=	ENSP00000354504.2:n.2243+23478A=
ENST00000361477.7:c.-449+23478A=	ENSP00000355116.4:n.-449+23478A=
ENST00000373986.7:c.1565+23478A=	ENSP00000363098.3:n.1565+23478A=
NM_014010.4:c.2243+23478A=	NP_054729.3:n.2243+23478A=
NM_001365068.1:c.2396+23478A= MANE Select	NP_001351997.1:n.2396+23478A=
NM_001365069.1:c.2384+23478A=	NP_001351998.1:n.2384+23478A=
NM_014010.5:c.2243+23478A=	NP_054729.3:n.2243+23478A=