Canonical Allele Identifier: CA2579546924
Gene: ANOS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731766_8731767dup , CM000685.2:g.8731766_8731767dup GRCh38
NC_000023.10:g.8699807_8699808dup , CM000685.1:g.8699807_8699808dup GRCh37
NC_000023.9:g.8659807_8659808dup NCBI36
NG_007088.1:g.5426_5427dup
NG_007088.2:g.5426_5427dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.207+69_207+70dup MANE Select ENSP00000262648.3:n.207+69_207+70dup
ENST00000262648.7:c.207+69_207+70dup ENSP00000262648.3:n.207+69_207+70dup
ENST00000619786.1:c.204+69_204+70dup ENSP00000478734.1:n.204+69_204+70dup
NM_000216.2:c.207+69_207+70dup NP_000207.2:n.207+69_207+70dup
XM_005274501.3:c.207+69_207+70dup XP_005274558.1:n.207+69_207+70dup
NM_000216.3:c.207+69_207+70dup NP_000207.2:n.207+69_207+70dup
XM_005274501.4:c.207+69_207+70dup XP_005274558.1:n.207+69_207+70dup
NM_000216.4:c.207+69_207+70dup MANE Select NP_000207.2:n.207+69_207+70dup