Canonical Allele Identifier: CA2414666299
Gene: ANOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8732018C= , CM000685.2:g.8732018C= GRCh38
NC_000023.10:g.8700059C= , CM000685.1:g.8700059C= GRCh37
NC_000023.9:g.8660059C= NCBI36
NG_007088.1:g.5169G=
NG_007088.2:g.5169G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.19G= MANE Select ENSP00000262648.3:p.Gly7=
ENST00000262648.7:c.19G= ENSP00000262648.3:p.Gly7=
ENST00000619786.1:c.19G= ENSP00000478734.1:p.Gly7=
NM_000216.2:c.19G= NP_000207.2:p.Gly7=
XM_005274501.3:c.19G= XP_005274558.1:p.Gly7=
NM_000216.3:c.19G= NP_000207.2:p.Gly7=
XM_005274501.4:c.19G= XP_005274558.1:p.Gly7=
NM_000216.4:c.19G= MANE Select NP_000207.2:p.Gly7=