Canonical Allele Identifier: CA2785708959

Gene: ASTN2 ASTN2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.116551937A>C , CM000671.2:g.116551937A>C	GRCh38
NC_000009.11:g.119314216A>C , CM000671.1:g.119314216A>C	GRCh37
NC_000009.10:g.118354037A>C	NCBI36
NG_021409.1:g.868102T>G
NG_021409.2:g.868121T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313400.9:c.3356-64437T>G (ASTN2) MANE Select	ENSP00000314038.4:n.3356-64437T>G
ENST00000361477.8:c.3203-64437T>G (ASTN2)	ENSP00000355116.5:n.3203-64437T>G
ENST00000288520.9:c.659-64437T>G (ASTN2)	ENSP00000288520.5:n.659-64437T>G
ENST00000313400.8:c.3356-64437T>G (ASTN2)	ENSP00000314038.4:n.3356-64437T>G
ENST00000341734.8:c.512-64437T>G (ASTN2)	ENSP00000339925.4:n.512-64437T>G
ENST00000361209.6:c.3203-64437T>G (ASTN2)	ENSP00000354504.2:n.3203-64437T>G
ENST00000361477.7:c.512-64437T>G (ASTN2)	ENSP00000355116.4:n.512-64437T>G
ENST00000373986.7:c.2525-64437T>G (ASTN2)	ENSP00000363098.3:n.2525-64437T>G
NM_001184734.1:c.512-64437T>G (ASTN2)	NP_001171663.1:n.512-64437T>G
NM_014010.4:c.3203-64437T>G (ASTN2)	NP_054729.3:n.3203-64437T>G
NM_198186.3:c.659-64437T>G (ASTN2)	NP_937829.3:n.659-64437T>G
NM_198187.3:c.512-64437T>G (ASTN2)	NP_937830.3:n.512-64437T>G
NM_198188.2:c.512-64437T>G (ASTN2)	NP_937831.1:n.512-64437T>G
NR_033973.1:n.1325-173A>C (ASTN2-AS1)
NM_001365068.1:c.3356-64437T>G (ASTN2) MANE Select	NP_001351997.1:n.3356-64437T>G
NM_001365069.1:c.3344-64437T>G (ASTN2)	NP_001351998.1:n.3344-64437T>G
NM_014010.5:c.3203-64437T>G (ASTN2)	NP_054729.3:n.3203-64437T>G