Canonical Allele Identifier: CA859158785
Gene: ASTN2 HGNC NCBI

Linked Data

dbSNP Id: rs1417548265

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.116571260_116571268del , CM000671.2:g.116571260_116571268del GRCh38
NC_000009.11:g.119333539_119333547del , CM000671.1:g.119333539_119333547del GRCh37
NC_000009.10:g.118373360_118373368del NCBI36
NG_021409.1:g.848772_848780del
NG_021409.2:g.848791_848799del

Transcript Alleles

HGVS Amino-acid change
ENST00000313400.9:c.3355+47057_3355+47065del MANE Select ENSP00000314038.4:n.3355+47057_3355+47065del
ENST00000361477.8:c.3202+47057_3202+47065del ENSP00000355116.5:n.3202+47057_3202+47065del
ENST00000288520.9:c.658+47057_658+47065del ENSP00000288520.5:n.658+47057_658+47065del
ENST00000313400.8:c.3355+47057_3355+47065del ENSP00000314038.4:n.3355+47057_3355+47065del
ENST00000341734.8:c.511+47057_511+47065del ENSP00000339925.4:n.511+47057_511+47065del
ENST00000361209.6:c.3202+47057_3202+47065del ENSP00000354504.2:n.3202+47057_3202+47065del
ENST00000361477.7:c.511+47057_511+47065del ENSP00000355116.4:n.511+47057_511+47065del
ENST00000373986.7:c.2524+47057_2524+47065del ENSP00000363098.3:n.2524+47057_2524+47065del
NM_001184734.1:c.511+47057_511+47065del NP_001171663.1:n.511+47057_511+47065del
NM_014010.4:c.3202+47057_3202+47065del NP_054729.3:n.3202+47057_3202+47065del
NM_198186.3:c.658+47057_658+47065del NP_937829.3:n.658+47057_658+47065del
NM_198187.3:c.511+47057_511+47065del NP_937830.3:n.511+47057_511+47065del
NM_198188.2:c.511+47057_511+47065del NP_937831.1:n.511+47057_511+47065del
NM_001365068.1:c.3355+47057_3355+47065del MANE Select NP_001351997.1:n.3355+47057_3355+47065del
NM_001365069.1:c.3343+47057_3343+47065del NP_001351998.1:n.3343+47057_3343+47065del
NM_014010.5:c.3202+47057_3202+47065del NP_054729.3:n.3202+47057_3202+47065del