Canonical Allele Identifier: CA1874956166

Gene: ASTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.116865885T= , CM000671.2:g.116865885T=	GRCh38
NC_000009.11:g.119628164T= , CM000671.1:g.119628164T=	GRCh37
NC_000009.10:g.118667985T=	NCBI36
NG_021409.1:g.554154A=
NG_021409.2:g.554173A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000313400.9:c.1890-2152A= MANE Select	ENSP00000314038.4:n.1890-2152A=
ENST00000361477.8:c.1737-2152A=	ENSP00000355116.5:n.1737-2152A=
ENST00000313400.8:c.1890-2152A=	ENSP00000314038.4:n.1890-2152A=
ENST00000361209.6:c.1737-2152A=	ENSP00000354504.2:n.1737-2152A=
ENST00000361477.7:c.-955-2152A=	ENSP00000355116.4:n.-955-2152A=
ENST00000373986.7:c.1059-2152A=	ENSP00000363098.3:n.1059-2152A=
NM_014010.4:c.1737-2152A=	NP_054729.3:n.1737-2152A=
NM_001365068.1:c.1890-2152A= MANE Select	NP_001351997.1:n.1890-2152A=
NM_001365069.1:c.1878-2152A=	NP_001351998.1:n.1878-2152A=
NM_014010.5:c.1737-2152A=	NP_054729.3:n.1737-2152A=