Canonical Allele Identifier: CA2414666199
Gene: ANOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731813_8731814delinsCG , CM000685.2:g.8731813_8731814delinsCG GRCh38
NC_000023.10:g.8699854_8699855delinsCG , CM000685.1:g.8699854_8699855delinsCG GRCh37
NC_000023.9:g.8659854_8659855delinsCG NCBI36
NG_007088.1:g.5373_5374delinsCG
NG_007088.2:g.5373_5374delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.207+16_207+17delinsCG MANE Select ENSP00000262648.3:n.207+16_207+17delinsCG
ENST00000262648.7:c.207+16_207+17delinsCG ENSP00000262648.3:n.207+16_207+17delinsCG
ENST00000619786.1:c.204+16_204+17delinsCG ENSP00000478734.1:n.204+16_204+17delinsCG
NM_000216.2:c.207+16_207+17delinsCG NP_000207.2:n.207+16_207+17delinsCG
XM_005274501.3:c.207+16_207+17delinsCG XP_005274558.1:n.207+16_207+17delinsCG
NM_000216.3:c.207+16_207+17delinsCG NP_000207.2:n.207+16_207+17delinsCG
XM_005274501.4:c.207+16_207+17delinsCG XP_005274558.1:n.207+16_207+17delinsCG
NM_000216.4:c.207+16_207+17delinsCG MANE Select NP_000207.2:n.207+16_207+17delinsCG