Canonical Allele Identifier: CA2500484391

Gene: ASTN2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117076965dup , CM000671.2:g.117076965dup	GRCh38
NC_000009.11:g.119839244dup , CM000671.1:g.119839244dup	GRCh37
NC_000009.10:g.118879065dup	NCBI36
NG_021409.1:g.343076dup
NG_021409.2:g.343095dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000313400.9:c.1276+19081dup MANE Select	ENSP00000314038.4:n.1276+19081dup
ENST00000361477.8:c.1123+19081dup	ENSP00000355116.5:n.1123+19081dup
ENST00000313400.8:c.1276+19081dup	ENSP00000314038.4:n.1276+19081dup
ENST00000361209.6:c.1123+19081dup	ENSP00000354504.2:n.1123+19081dup
ENST00000361477.7:c.-1569+19081dup	ENSP00000355116.4:n.-1569+19081dup
ENST00000373986.7:c.457+19081dup	ENSP00000363098.3:n.457+19081dup
NM_014010.4:c.1123+19081dup	NP_054729.3:n.1123+19081dup
NM_001365068.1:c.1276+19081dup MANE Select	NP_001351997.1:n.1276+19081dup
NM_001365069.1:c.1276+19081dup	NP_001351998.1:n.1276+19081dup
NM_014010.5:c.1123+19081dup	NP_054729.3:n.1123+19081dup