Canonical Allele Identifier: CA2579546827
Gene: ANOS1 HGNC NCBI

Linked Data

gnomAD v4: X-8587745-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8587745G>T , CM000685.2:g.8587745G>T GRCh38
NC_000023.10:g.8555786G>T , CM000685.1:g.8555786G>T GRCh37
NC_000023.9:g.8515786G>T NCBI36
NG_007088.1:g.149442C>A
NG_007088.2:g.149442C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.726+49C>A MANE Select ENSP00000262648.3:n.726+49C>A
ENST00000262648.7:c.726+49C>A ENSP00000262648.3:n.726+49C>A
ENST00000619786.1:c.723+49C>A ENSP00000478734.1:n.723+49C>A
NM_000216.2:c.726+49C>A NP_000207.2:n.726+49C>A
XM_005274501.3:c.726+49C>A XP_005274558.1:n.726+49C>A
NM_000216.3:c.726+49C>A NP_000207.2:n.726+49C>A
XM_005274501.4:c.726+49C>A XP_005274558.1:n.726+49C>A
NM_000216.4:c.726+49C>A MANE Select NP_000207.2:n.726+49C>A