Canonical Allele Identifier: CA1874956229
Gene: ASTN2 HGNC NCBI

Linked Data

dbSNP Id: rs1833006083

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.116866023_116866025del , CM000671.2:g.116866023_116866025del GRCh38
NC_000009.11:g.119628302_119628304del , CM000671.1:g.119628302_119628304del GRCh37
NC_000009.10:g.118668123_118668125del NCBI36
NG_021409.1:g.554016_554018del
NG_021409.2:g.554035_554037del

Transcript Alleles

HGVS Amino-acid change
ENST00000313400.9:c.1890-2290_1890-2288del MANE Select ENSP00000314038.4:n.1890-2290_1890-2288de...
ENST00000361477.8:c.1737-2290_1737-2288del ENSP00000355116.5:n.1737-2290_1737-2288de...
ENST00000313400.8:c.1890-2290_1890-2288del ENSP00000314038.4:n.1890-2290_1890-2288de...
ENST00000361209.6:c.1737-2290_1737-2288del ENSP00000354504.2:n.1737-2290_1737-2288de...
ENST00000361477.7:c.-955-2290_-955-2288del ENSP00000355116.4:n.-955-2290_-955-2288de...
ENST00000373986.7:c.1059-2290_1059-2288del ENSP00000363098.3:n.1059-2290_1059-2288de...
NM_014010.4:c.1737-2290_1737-2288del NP_054729.3:n.1737-2290_1737-2288del
NM_001365068.1:c.1890-2290_1890-2288del MANE Select NP_001351997.1:n.1890-2290_1890-2288del
NM_001365069.1:c.1878-2290_1878-2288del NP_001351998.1:n.1878-2290_1878-2288del
NM_014010.5:c.1737-2290_1737-2288del NP_054729.3:n.1737-2290_1737-2288del