Canonical Allele Identifier: CA2528746527

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618207_186618208del , CM000665.2:g.186618207_186618208del	GRCh38
NC_000003.11:g.186335996_186335997del , CM000665.1:g.186335996_186335997del	GRCh37
NC_000003.10:g.187818690_187818691del	NCBI36
NG_011436.1:g.10147_10148del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-329_574-328del MANE Select	ENSP00000393887.2:n.574-329_574-328del
ENST00000273784.5:c.577-329_577-328del	ENSP00000273784.5:n.577-329_577-328del
ENST00000411641.6:c.574-329_574-328del	ENSP00000393887.2:n.574-329_574-328del
NM_001622.2:c.574-329_574-328del	NP_001613.2:n.574-329_574-328del
NM_001354571.1:c.577-329_577-328del	NP_001341500.1:n.577-329_577-328del
NM_001354572.1:c.571-329_571-328del	NP_001341501.1:n.571-329_571-328del
NM_001354573.1:c.574-329_574-328del	NP_001341502.1:n.574-329_574-328del
NM_001622.3:c.574-329_574-328del	NP_001613.2:n.574-329_574-328del
NM_001622.4:c.574-329_574-328del MANE Select	NP_001613.2:n.574-329_574-328del
NM_001354571.2:c.577-329_577-328del	NP_001341500.1:n.577-329_577-328del
NM_001354572.2:c.571-329_571-328del	NP_001341501.1:n.571-329_571-328del
NM_001354573.2:c.574-329_574-328del	NP_001341502.1:n.574-329_574-328del