Canonical Allele Identifier: CA640857322
Gene: ANOS1 HGNC NCBI

Linked Data

dbSNP Id: rs1203944318

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8732061_8732066del , CM000685.2:g.8732061_8732066del GRCh38
NC_000023.10:g.8700102_8700107del , CM000685.1:g.8700102_8700107del GRCh37
NC_000023.9:g.8660102_8660107del NCBI36
NG_007088.1:g.5135_5140del
NG_007088.2:g.5135_5140del

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.-16_-11del MANE Select ENSP00000262648.3:n.-16_-11del
ENST00000262648.7:c.-16_-11del ENSP00000262648.3:n.-16_-11del
ENST00000619786.1:c.-16_-11del ENSP00000478734.1:n.-16_-11del
NM_000216.2:c.-16_-11del NP_000207.2:n.-16_-11del
XM_005274501.3:c.-16_-11del XP_005274558.1:n.-16_-11del
NM_000216.3:c.-16_-11del NP_000207.2:n.-16_-11del
XM_005274501.4:c.-16_-11del XP_005274558.1:n.-16_-11del
NM_000216.4:c.-16_-11del MANE Select NP_000207.2:n.-16_-11del