Canonical Allele Identifier: CA2668958447

Gene: AHSG

Linked Data

• gnomAD v4: 3-186617968-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617969_186617970del , CM000665.2:g.186617969_186617970del	GRCh38
NC_000003.11:g.186335758_186335759del , CM000665.1:g.186335758_186335759del	GRCh37
NC_000003.10:g.187818452_187818453del	NCBI36
NG_011436.1:g.9909_9910del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-567_574-566del MANE Select	ENSP00000393887.2:n.574-567_574-566del
ENST00000273784.5:c.577-567_577-566del	ENSP00000273784.5:n.577-567_577-566del
ENST00000411641.6:c.574-567_574-566del	ENSP00000393887.2:n.574-567_574-566del
ENST00000478441.1:n.1249_1250del
NM_001622.2:c.574-567_574-566del	NP_001613.2:n.574-567_574-566del
NM_001354571.1:c.577-567_577-566del	NP_001341500.1:n.577-567_577-566del
NM_001354572.1:c.571-567_571-566del	NP_001341501.1:n.571-567_571-566del
NM_001354573.1:c.574-567_574-566del	NP_001341502.1:n.574-567_574-566del
NM_001622.3:c.574-567_574-566del	NP_001613.2:n.574-567_574-566del
NM_001622.4:c.574-567_574-566del MANE Select	NP_001613.2:n.574-567_574-566del
NM_001354571.2:c.577-567_577-566del	NP_001341500.1:n.577-567_577-566del
NM_001354572.2:c.571-567_571-566del	NP_001341501.1:n.571-567_571-566del
NM_001354573.2:c.574-567_574-566del	NP_001341502.1:n.574-567_574-566del