Canonical Allele Identifier: CA1874956184

Gene: ASTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.116865919A= , CM000671.2:g.116865919A=	GRCh38
NC_000009.11:g.119628198A= , CM000671.1:g.119628198A=	GRCh37
NC_000009.10:g.118668019A=	NCBI36
NG_021409.1:g.554120T=
NG_021409.2:g.554139T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000313400.9:c.1890-2186T= MANE Select	ENSP00000314038.4:n.1890-2186T=
ENST00000361477.8:c.1737-2186T=	ENSP00000355116.5:n.1737-2186T=
ENST00000313400.8:c.1890-2186T=	ENSP00000314038.4:n.1890-2186T=
ENST00000361209.6:c.1737-2186T=	ENSP00000354504.2:n.1737-2186T=
ENST00000361477.7:c.-955-2186T=	ENSP00000355116.4:n.-955-2186T=
ENST00000373986.7:c.1059-2186T=	ENSP00000363098.3:n.1059-2186T=
NM_014010.4:c.1737-2186T=	NP_054729.3:n.1737-2186T=
NM_001365068.1:c.1890-2186T= MANE Select	NP_001351997.1:n.1890-2186T=
NM_001365069.1:c.1878-2186T=	NP_001351998.1:n.1878-2186T=
NM_014010.5:c.1737-2186T=	NP_054729.3:n.1737-2186T=