Canonical Allele Identifier: CA2549708339

Gene: AHSG

Linked Data

• gnomAD v4: 3-186617960-TGTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617961_186617964del , CM000665.2:g.186617961_186617964del	GRCh38
NC_000003.11:g.186335750_186335753del , CM000665.1:g.186335750_186335753del	GRCh37
NC_000003.10:g.187818444_187818447del	NCBI36
NG_011436.1:g.9901_9904del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.574-575_574-572del MANE Select	ENSP00000393887.2:n.574-575_574-572del
ENST00000273784.5:c.577-575_577-572del	ENSP00000273784.5:n.577-575_577-572del
ENST00000411641.6:c.574-575_574-572del	ENSP00000393887.2:n.574-575_574-572del
ENST00000478441.1:n.1241_1244del
NM_001622.2:c.574-575_574-572del	NP_001613.2:n.574-575_574-572del
NM_001354571.1:c.577-575_577-572del	NP_001341500.1:n.577-575_577-572del
NM_001354572.1:c.571-575_571-572del	NP_001341501.1:n.571-575_571-572del
NM_001354573.1:c.574-575_574-572del	NP_001341502.1:n.574-575_574-572del
NM_001622.3:c.574-575_574-572del	NP_001613.2:n.574-575_574-572del
NM_001622.4:c.574-575_574-572del MANE Select	NP_001613.2:n.574-575_574-572del
NM_001354571.2:c.577-575_577-572del	NP_001341500.1:n.577-575_577-572del
NM_001354572.2:c.571-575_571-572del	NP_001341501.1:n.571-575_571-572del
NM_001354573.2:c.574-575_574-572del	NP_001341502.1:n.574-575_574-572del