Canonical Allele Identifier: CA2693053826
Gene: ANOS1 HGNC NCBI

Linked Data

gnomAD v4: X-8587733-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.8587733C>A , CM000685.2:g.8587733C>A GRCh38
NC_000023.10:g.8555774C>A , CM000685.1:g.8555774C>A GRCh37
NC_000023.9:g.8515774C>A NCBI36
NG_007088.1:g.149454G>T
NG_007088.2:g.149454G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000262648.8:c.726+61G>T MANE Select ENSP00000262648.3:n.726+61G>T
ENST00000262648.7:c.726+61G>T ENSP00000262648.3:n.726+61G>T
ENST00000619786.1:c.723+61G>T ENSP00000478734.1:n.723+61G>T
NM_000216.2:c.726+61G>T NP_000207.2:n.726+61G>T
XM_005274501.3:c.726+61G>T XP_005274558.1:n.726+61G>T
NM_000216.3:c.726+61G>T NP_000207.2:n.726+61G>T
XM_005274501.4:c.726+61G>T XP_005274558.1:n.726+61G>T
NM_000216.4:c.726+61G>T MANE Select NP_000207.2:n.726+61G>T