Canonical Allele Identifier: CA2414666126

Gene: ANOS1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.8731624_8731627delinsGCTT , CM000685.2:g.8731624_8731627delinsGCTT	GRCh38
NC_000023.10:g.8699665_8699668delinsGCTT , CM000685.1:g.8699665_8699668delinsGCTT	GRCh37
NC_000023.9:g.8659665_8659668delinsGCTT	NCBI36
NG_007088.1:g.5560_5563delinsAAGC
NG_007088.2:g.5560_5563delinsAAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262648.8:c.207+203_207+206delinsAAGC MANE Select	ENSP00000262648.3:n.207+203_207+206delinsAAGC
ENST00000262648.7:c.207+203_207+206delinsAAGC	ENSP00000262648.3:n.207+203_207+206delinsAAGC
ENST00000619786.1:c.204+203_204+206delinsAAGC	ENSP00000478734.1:n.204+203_204+206delinsAAGC
NM_000216.2:c.207+203_207+206delinsAAGC	NP_000207.2:n.207+203_207+206delinsAAGC
XM_005274501.3:c.207+203_207+206delinsAAGC	XP_005274558.1:n.207+203_207+206delinsAAGC
NM_000216.3:c.207+203_207+206delinsAAGC	NP_000207.2:n.207+203_207+206delinsAAGC
XM_005274501.4:c.207+203_207+206delinsAAGC	XP_005274558.1:n.207+203_207+206delinsAAGC
NM_000216.4:c.207+203_207+206delinsAAGC MANE Select	NP_000207.2:n.207+203_207+206delinsAAGC