Canonical Allele Identifier: CA1874811007
Gene: ASTN2 HGNC NCBI
ASTN2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs13290997

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.116551938A>T , CM000671.2:g.116551938A>T GRCh38
NC_000009.11:g.119314217A>T , CM000671.1:g.119314217A>T GRCh37
NC_000009.10:g.118354038A>T NCBI36
NG_021409.1:g.868101T>A
NG_021409.2:g.868120T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000313400.9:c.3356-64438T>A (ASTN2) MANE Select ENSP00000314038.4:n.3356-64438T>A
ENST00000361477.8:c.3203-64438T>A (ASTN2) ENSP00000355116.5:n.3203-64438T>A
ENST00000288520.9:c.659-64438T>A (ASTN2) ENSP00000288520.5:n.659-64438T>A
ENST00000313400.8:c.3356-64438T>A (ASTN2) ENSP00000314038.4:n.3356-64438T>A
ENST00000341734.8:c.512-64438T>A (ASTN2) ENSP00000339925.4:n.512-64438T>A
ENST00000361209.6:c.3203-64438T>A (ASTN2) ENSP00000354504.2:n.3203-64438T>A
ENST00000361477.7:c.512-64438T>A (ASTN2) ENSP00000355116.4:n.512-64438T>A
ENST00000373986.7:c.2525-64438T>A (ASTN2) ENSP00000363098.3:n.2525-64438T>A
NM_001184734.1:c.512-64438T>A (ASTN2) NP_001171663.1:n.512-64438T>A
NM_014010.4:c.3203-64438T>A (ASTN2) NP_054729.3:n.3203-64438T>A
NM_198186.3:c.659-64438T>A (ASTN2) NP_937829.3:n.659-64438T>A
NM_198187.3:c.512-64438T>A (ASTN2) NP_937830.3:n.512-64438T>A
NM_198188.2:c.512-64438T>A (ASTN2) NP_937831.1:n.512-64438T>A
NR_033973.1:n.1325-172A>T (ASTN2-AS1)
NM_001365068.1:c.3356-64438T>A (ASTN2) MANE Select NP_001351997.1:n.3356-64438T>A
NM_001365069.1:c.3344-64438T>A (ASTN2) NP_001351998.1:n.3344-64438T>A
NM_014010.5:c.3203-64438T>A (ASTN2) NP_054729.3:n.3203-64438T>A