Canonical Allele Identifier: CA2414666152

Gene: ANOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.8731710_8731711delinsAG , CM000685.2:g.8731710_8731711delinsAG	GRCh38
NC_000023.10:g.8699751_8699752delinsAG , CM000685.1:g.8699751_8699752delinsAG	GRCh37
NC_000023.9:g.8659751_8659752delinsAG	NCBI36
NG_007088.1:g.5476_5477delinsCT
NG_007088.2:g.5476_5477delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262648.8:c.207+119_207+120delinsCT MANE Select	ENSP00000262648.3:n.207+119_207+120delinsCT
ENST00000262648.7:c.207+119_207+120delinsCT	ENSP00000262648.3:n.207+119_207+120delinsCT
ENST00000619786.1:c.204+119_204+120delinsCT	ENSP00000478734.1:n.204+119_204+120delinsCT
NM_000216.2:c.207+119_207+120delinsCT	NP_000207.2:n.207+119_207+120delinsCT
XM_005274501.3:c.207+119_207+120delinsCT	XP_005274558.1:n.207+119_207+120delinsCT
NM_000216.3:c.207+119_207+120delinsCT	NP_000207.2:n.207+119_207+120delinsCT
XM_005274501.4:c.207+119_207+120delinsCT	XP_005274558.1:n.207+119_207+120delinsCT
NM_000216.4:c.207+119_207+120delinsCT MANE Select	NP_000207.2:n.207+119_207+120delinsCT