Canonical Allele Identifier: CA1875058147
Gene: ASTN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117076968A= , CM000671.2:g.117076968A= GRCh38
NC_000009.11:g.119839247A= , CM000671.1:g.119839247A= GRCh37
NC_000009.10:g.118879068A= NCBI36
NG_021409.1:g.343071T=
NG_021409.2:g.343090T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313400.9:c.1276+19076T= MANE Select ENSP00000314038.4:n.1276+19076T=
ENST00000361477.8:c.1123+19076T= ENSP00000355116.5:n.1123+19076T=
ENST00000313400.8:c.1276+19076T= ENSP00000314038.4:n.1276+19076T=
ENST00000361209.6:c.1123+19076T= ENSP00000354504.2:n.1123+19076T=
ENST00000361477.7:c.-1569+19076T= ENSP00000355116.4:n.-1569+19076T=
ENST00000373986.7:c.457+19076T= ENSP00000363098.3:n.457+19076T=
NM_014010.4:c.1123+19076T= NP_054729.3:n.1123+19076T=
NM_001365068.1:c.1276+19076T= MANE Select NP_001351997.1:n.1276+19076T=
NM_001365069.1:c.1276+19076T= NP_001351998.1:n.1276+19076T=
NM_014010.5:c.1123+19076T= NP_054729.3:n.1123+19076T=