Canonical Allele Identifier: CA1874956239

Gene: ASTN2

Linked Data

• dbSNP Id: rs1833006508

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.116866050_116866053del , CM000671.2:g.116866050_116866053del	GRCh38
NC_000009.11:g.119628329_119628332del , CM000671.1:g.119628329_119628332del	GRCh37
NC_000009.10:g.118668150_118668153del	NCBI36
NG_021409.1:g.553990_553993del
NG_021409.2:g.554009_554012del

Transcript Alleles

HGVS	Amino-acid change
ENST00000313400.9:c.1890-2316_1890-2313del MANE Select	ENSP00000314038.4:n.1890-2316_1890-2313del
ENST00000361477.8:c.1737-2316_1737-2313del	ENSP00000355116.5:n.1737-2316_1737-2313del
ENST00000313400.8:c.1890-2316_1890-2313del	ENSP00000314038.4:n.1890-2316_1890-2313del
ENST00000361209.6:c.1737-2316_1737-2313del	ENSP00000354504.2:n.1737-2316_1737-2313del
ENST00000361477.7:c.-955-2316_-955-2313del	ENSP00000355116.4:n.-955-2316_-955-2313del
ENST00000373986.7:c.1059-2316_1059-2313del	ENSP00000363098.3:n.1059-2316_1059-2313del
NM_014010.4:c.1737-2316_1737-2313del	NP_054729.3:n.1737-2316_1737-2313del
NM_001365068.1:c.1890-2316_1890-2313del MANE Select	NP_001351997.1:n.1890-2316_1890-2313del
NM_001365069.1:c.1878-2316_1878-2313del	NP_001351998.1:n.1878-2316_1878-2313del
NM_014010.5:c.1737-2316_1737-2313del	NP_054729.3:n.1737-2316_1737-2313del