Canonical Allele Identifier: CA1427016913

Gene: AHSG

Linked Data

• dbSNP Id: rs1716245795

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186614788_186614794del , CM000665.2:g.186614788_186614794del	GRCh38
NC_000003.11:g.186332577_186332583del , CM000665.1:g.186332577_186332583del	GRCh37
NC_000003.10:g.187815271_187815277del	NCBI36
NG_011436.1:g.6728_6734del

Transcript Alleles

HGVS	Amino-acid change
ENST00000411641.7:c.214-897_214-891del MANE Select	ENSP00000393887.2:n.214-897_214-891del
ENST00000273784.5:c.214-897_214-891del	ENSP00000273784.5:n.214-897_214-891del
ENST00000411641.6:c.214-897_214-891del	ENSP00000393887.2:n.214-897_214-891del
ENST00000478441.1:n.271-897_271-891del
NM_001622.2:c.214-897_214-891del	NP_001613.2:n.214-897_214-891del
NM_001354571.1:c.214-897_214-891del	NP_001341500.1:n.214-897_214-891del
NM_001354572.1:c.214-900_214-894del	NP_001341501.1:n.214-900_214-894del
NM_001354573.1:c.214-897_214-891del	NP_001341502.1:n.214-897_214-891del
NM_001622.3:c.214-897_214-891del	NP_001613.2:n.214-897_214-891del
NM_001622.4:c.214-897_214-891del MANE Select	NP_001613.2:n.214-897_214-891del
NM_001354571.2:c.214-897_214-891del	NP_001341500.1:n.214-897_214-891del
NM_001354572.2:c.214-900_214-894del	NP_001341501.1:n.214-900_214-894del
NM_001354573.2:c.214-897_214-891del	NP_001341502.1:n.214-897_214-891del