Canonical Allele Identifier: CA2414666145
Gene: ANOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8731693C= , CM000685.2:g.8731693C= GRCh38
NC_000023.10:g.8699734C= , CM000685.1:g.8699734C= GRCh37
NC_000023.9:g.8659734C= NCBI36
NG_007088.1:g.5494G=
NG_007088.2:g.5494G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262648.8:c.207+137G= MANE Select ENSP00000262648.3:n.207+137G=
ENST00000262648.7:c.207+137G= ENSP00000262648.3:n.207+137G=
ENST00000619786.1:c.204+137G= ENSP00000478734.1:n.204+137G=
NM_000216.2:c.207+137G= NP_000207.2:n.207+137G=
XM_005274501.3:c.207+137G= XP_005274558.1:n.207+137G=
NM_000216.3:c.207+137G= NP_000207.2:n.207+137G=
XM_005274501.4:c.207+137G= XP_005274558.1:n.207+137G=
NM_000216.4:c.207+137G= MANE Select NP_000207.2:n.207+137G=
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