Canonical Allele Identifier: CA2668958416

Gene: AHSG

Linked Data

• gnomAD v4: 3-186617965-TTCTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617966_186617969del , CM000665.2:g.186617966_186617969del	GRCh38
NC_000003.11:g.186335755_186335758del , CM000665.1:g.186335755_186335758del	GRCh37
NC_000003.10:g.187818449_187818452del	NCBI36
NG_011436.1:g.9906_9909del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-570_574-567del MANE Select	ENSP00000393887.2:n.574-570_574-567del
ENST00000273784.5:c.577-570_577-567del	ENSP00000273784.5:n.577-570_577-567del
ENST00000411641.6:c.574-570_574-567del	ENSP00000393887.2:n.574-570_574-567del
ENST00000478441.1:n.1246_1249del
NM_001622.2:c.574-570_574-567del	NP_001613.2:n.574-570_574-567del
NM_001354571.1:c.577-570_577-567del	NP_001341500.1:n.577-570_577-567del
NM_001354572.1:c.571-570_571-567del	NP_001341501.1:n.571-570_571-567del
NM_001354573.1:c.574-570_574-567del	NP_001341502.1:n.574-570_574-567del
NM_001622.3:c.574-570_574-567del	NP_001613.2:n.574-570_574-567del
NM_001622.4:c.574-570_574-567del MANE Select	NP_001613.2:n.574-570_574-567del
NM_001354571.2:c.577-570_577-567del	NP_001341500.1:n.577-570_577-567del
NM_001354572.2:c.571-570_571-567del	NP_001341501.1:n.571-570_571-567del
NM_001354573.2:c.574-570_574-567del	NP_001341502.1:n.574-570_574-567del