Canonical Allele Identifier: CA2579546822
Gene: ANOS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8587712A>T , CM000685.2:g.8587712A>T GRCh38
NC_000023.10:g.8555753A>T , CM000685.1:g.8555753A>T GRCh37
NC_000023.9:g.8515753A>T NCBI36
NG_007088.1:g.149475T>A
NG_007088.2:g.149475T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.726+82T>A MANE Select ENSP00000262648.3:n.726+82T>A
ENST00000262648.7:c.726+82T>A ENSP00000262648.3:n.726+82T>A
ENST00000619786.1:c.723+82T>A ENSP00000478734.1:n.723+82T>A
NM_000216.2:c.726+82T>A NP_000207.2:n.726+82T>A
XM_005274501.3:c.726+82T>A XP_005274558.1:n.726+82T>A
NM_000216.3:c.726+82T>A NP_000207.2:n.726+82T>A
XM_005274501.4:c.726+82T>A XP_005274558.1:n.726+82T>A
NM_000216.4:c.726+82T>A MANE Select NP_000207.2:n.726+82T>A
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