Canonical Allele Identifier: CA2759779121

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186614815_186614820del , CM000665.2:g.186614815_186614820del	GRCh38
NC_000003.11:g.186332604_186332609del , CM000665.1:g.186332604_186332609del	GRCh37
NC_000003.10:g.187815298_187815303del	NCBI36
NG_011436.1:g.6755_6760del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.214-870_214-865del MANE Select	ENSP00000393887.2:n.214-870_214-865del
ENST00000273784.5:c.214-870_214-865del	ENSP00000273784.5:n.214-870_214-865del
ENST00000411641.6:c.214-870_214-865del	ENSP00000393887.2:n.214-870_214-865del
ENST00000478441.1:n.271-870_271-865del
NM_001622.2:c.214-870_214-865del	NP_001613.2:n.214-870_214-865del
NM_001354571.1:c.214-870_214-865del	NP_001341500.1:n.214-870_214-865del
NM_001354572.1:c.214-873_214-868del	NP_001341501.1:n.214-873_214-868del
NM_001354573.1:c.214-870_214-865del	NP_001341502.1:n.214-870_214-865del
NM_001622.3:c.214-870_214-865del	NP_001613.2:n.214-870_214-865del
NM_001622.4:c.214-870_214-865del MANE Select	NP_001613.2:n.214-870_214-865del
NM_001354571.2:c.214-870_214-865del	NP_001341500.1:n.214-870_214-865del
NM_001354572.2:c.214-873_214-868del	NP_001341501.1:n.214-873_214-868del
NM_001354573.2:c.214-870_214-865del	NP_001341502.1:n.214-870_214-865del