Canonical Allele Identifier: CA2693053827
Gene: ANOS1 HGNC NCBI

Linked Data

gnomAD v4: X-8587737-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8587737G>C , CM000685.2:g.8587737G>C GRCh38
NC_000023.10:g.8555778G>C , CM000685.1:g.8555778G>C GRCh37
NC_000023.9:g.8515778G>C NCBI36
NG_007088.1:g.149450C>G
NG_007088.2:g.149450C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.726+57C>G MANE Select ENSP00000262648.3:n.726+57C>G
ENST00000262648.7:c.726+57C>G ENSP00000262648.3:n.726+57C>G
ENST00000619786.1:c.723+57C>G ENSP00000478734.1:n.723+57C>G
NM_000216.2:c.726+57C>G NP_000207.2:n.726+57C>G
XM_005274501.3:c.726+57C>G XP_005274558.1:n.726+57C>G
NM_000216.3:c.726+57C>G NP_000207.2:n.726+57C>G
XM_005274501.4:c.726+57C>G XP_005274558.1:n.726+57C>G
NM_000216.4:c.726+57C>G MANE Select NP_000207.2:n.726+57C>G
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