Canonical Allele Identifier: CA1874811051
Gene: ASTN2 HGNC NCBI
ASTN2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1852369721

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.116551985C>G , CM000671.2:g.116551985C>G GRCh38
NC_000009.11:g.119314264C>G , CM000671.1:g.119314264C>G GRCh37
NC_000009.10:g.118354085C>G NCBI36
NG_021409.1:g.868054G>C
NG_021409.2:g.868073G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000313400.9:c.3356-64485G>C (ASTN2) MANE Select ENSP00000314038.4:n.3356-64485G>C
ENST00000361477.8:c.3203-64485G>C (ASTN2) ENSP00000355116.5:n.3203-64485G>C
ENST00000288520.9:c.659-64485G>C (ASTN2) ENSP00000288520.5:n.659-64485G>C
ENST00000313400.8:c.3356-64485G>C (ASTN2) ENSP00000314038.4:n.3356-64485G>C
ENST00000341734.8:c.512-64485G>C (ASTN2) ENSP00000339925.4:n.512-64485G>C
ENST00000361209.6:c.3203-64485G>C (ASTN2) ENSP00000354504.2:n.3203-64485G>C
ENST00000361477.7:c.512-64485G>C (ASTN2) ENSP00000355116.4:n.512-64485G>C
ENST00000373986.7:c.2525-64485G>C (ASTN2) ENSP00000363098.3:n.2525-64485G>C
NM_001184734.1:c.512-64485G>C (ASTN2) NP_001171663.1:n.512-64485G>C
NM_014010.4:c.3203-64485G>C (ASTN2) NP_054729.3:n.3203-64485G>C
NM_198186.3:c.659-64485G>C (ASTN2) NP_937829.3:n.659-64485G>C
NM_198187.3:c.512-64485G>C (ASTN2) NP_937830.3:n.512-64485G>C
NM_198188.2:c.512-64485G>C (ASTN2) NP_937831.1:n.512-64485G>C
NR_033973.1:n.1325-125C>G (ASTN2-AS1)
NM_001365068.1:c.3356-64485G>C (ASTN2) MANE Select NP_001351997.1:n.3356-64485G>C
NM_001365069.1:c.3344-64485G>C (ASTN2) NP_001351998.1:n.3344-64485G>C
NM_014010.5:c.3203-64485G>C (ASTN2) NP_054729.3:n.3203-64485G>C