Canonical Allele Identifier: CA1427018455

Gene: AHSG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186618007_186618008delinsAT , CM000665.2:g.186618007_186618008delinsAT	GRCh38
NC_000003.11:g.186335796_186335797delinsAT , CM000665.1:g.186335796_186335797delinsAT	GRCh37
NC_000003.10:g.187818490_187818491delinsAT	NCBI36
NG_011436.1:g.9947_9948delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-529_574-528delinsAT MANE Select	ENSP00000393887.2:n.574-529_574-528delinsAT
ENST00000273784.5:c.577-529_577-528delinsAT	ENSP00000273784.5:n.577-529_577-528delinsAT
ENST00000411641.6:c.574-529_574-528delinsAT	ENSP00000393887.2:n.574-529_574-528delinsAT
NM_001622.2:c.574-529_574-528delinsAT	NP_001613.2:n.574-529_574-528delinsAT
NM_001354571.1:c.577-529_577-528delinsAT	NP_001341500.1:n.577-529_577-528delinsAT
NM_001354572.1:c.571-529_571-528delinsAT	NP_001341501.1:n.571-529_571-528delinsAT
NM_001354573.1:c.574-529_574-528delinsAT	NP_001341502.1:n.574-529_574-528delinsAT
NM_001622.3:c.574-529_574-528delinsAT	NP_001613.2:n.574-529_574-528delinsAT
NM_001622.4:c.574-529_574-528delinsAT MANE Select	NP_001613.2:n.574-529_574-528delinsAT
NM_001354571.2:c.577-529_577-528delinsAT	NP_001341500.1:n.577-529_577-528delinsAT
NM_001354572.2:c.571-529_571-528delinsAT	NP_001341501.1:n.571-529_571-528delinsAT
NM_001354573.2:c.574-529_574-528delinsAT	NP_001341502.1:n.574-529_574-528delinsAT