Canonical Allele Identifier: CA2668958495

Gene: AHSG

Linked Data

• gnomAD v4: 3-186617972-AACATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617973_186617977del , CM000665.2:g.186617973_186617977del	GRCh38
NC_000003.11:g.186335762_186335766del , CM000665.1:g.186335762_186335766del	GRCh37
NC_000003.10:g.187818456_187818460del	NCBI36
NG_011436.1:g.9913_9917del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-563_574-559del MANE Select	ENSP00000393887.2:n.574-563_574-559del
ENST00000273784.5:c.577-563_577-559del	ENSP00000273784.5:n.577-563_577-559del
ENST00000411641.6:c.574-563_574-559del	ENSP00000393887.2:n.574-563_574-559del
ENST00000478441.1:n.1253_1257del
NM_001622.2:c.574-563_574-559del	NP_001613.2:n.574-563_574-559del
NM_001354571.1:c.577-563_577-559del	NP_001341500.1:n.577-563_577-559del
NM_001354572.1:c.571-563_571-559del	NP_001341501.1:n.571-563_571-559del
NM_001354573.1:c.574-563_574-559del	NP_001341502.1:n.574-563_574-559del
NM_001622.3:c.574-563_574-559del	NP_001613.2:n.574-563_574-559del
NM_001622.4:c.574-563_574-559del MANE Select	NP_001613.2:n.574-563_574-559del
NM_001354571.2:c.577-563_577-559del	NP_001341500.1:n.577-563_577-559del
NM_001354572.2:c.571-563_571-559del	NP_001341501.1:n.571-563_571-559del
NM_001354573.2:c.574-563_574-559del	NP_001341502.1:n.574-563_574-559del