Canonical Allele Identifier: CA2414666127

Gene: ANOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.8731628_8731631delinsCTTT , CM000685.2:g.8731628_8731631delinsCTTT	GRCh38
NC_000023.10:g.8699669_8699672delinsCTTT , CM000685.1:g.8699669_8699672delinsCTTT	GRCh37
NC_000023.9:g.8659669_8659672delinsCTTT	NCBI36
NG_007088.1:g.5556_5559delinsAAAG
NG_007088.2:g.5556_5559delinsAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262648.8:c.207+199_207+202delinsAAAG MANE Select	ENSP00000262648.3:n.207+199_207+202delinsAAAG
ENST00000262648.7:c.207+199_207+202delinsAAAG	ENSP00000262648.3:n.207+199_207+202delinsAAAG
ENST00000619786.1:c.204+199_204+202delinsAAAG	ENSP00000478734.1:n.204+199_204+202delinsAAAG
NM_000216.2:c.207+199_207+202delinsAAAG	NP_000207.2:n.207+199_207+202delinsAAAG
XM_005274501.3:c.207+199_207+202delinsAAAG	XP_005274558.1:n.207+199_207+202delinsAAAG
NM_000216.3:c.207+199_207+202delinsAAAG	NP_000207.2:n.207+199_207+202delinsAAAG
XM_005274501.4:c.207+199_207+202delinsAAAG	XP_005274558.1:n.207+199_207+202delinsAAAG
NM_000216.4:c.207+199_207+202delinsAAAG MANE Select	NP_000207.2:n.207+199_207+202delinsAAAG