Canonical Allele Identifier: CA1875100266

Gene: ASTN2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117164147T>C , CM000671.2:g.117164147T>C	GRCh38
NC_000009.11:g.119926426T>C , CM000671.1:g.119926426T>C	GRCh37
NC_000009.10:g.118966247T>C	NCBI36
NG_021409.1:g.255892A>G
NG_021409.2:g.255911A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313400.9:c.1016-22669A>G MANE Select	ENSP00000314038.4:n.1016-22669A>G
ENST00000361477.8:c.1015+50211A>G	ENSP00000355116.5:n.1015+50211A>G
ENST00000313400.8:c.1016-22669A>G	ENSP00000314038.4:n.1016-22669A>G
ENST00000361209.6:c.1015+50211A>G	ENSP00000354504.2:n.1015+50211A>G
ENST00000361477.7:c.-1677+50211A>G	ENSP00000355116.4:n.-1677+50211A>G
ENST00000373986.7:c.197-22669A>G	ENSP00000363098.3:n.197-22669A>G
NM_014010.4:c.1015+50211A>G	NP_054729.3:n.1015+50211A>G
NM_001365068.1:c.1016-22669A>G MANE Select	NP_001351997.1:n.1016-22669A>G
NM_001365069.1:c.1016-22669A>G	NP_001351998.1:n.1016-22669A>G
NM_014010.5:c.1015+50211A>G	NP_054729.3:n.1015+50211A>G