Canonical Allele Identifier: CA2668958076

Gene: AHSG

Linked Data

• gnomAD v4: 3-186617848-GCACA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.186617849_186617852del , CM000665.2:g.186617849_186617852del	GRCh38
NC_000003.11:g.186335638_186335641del , CM000665.1:g.186335638_186335641del	GRCh37
NC_000003.10:g.187818332_187818335del	NCBI36
NG_011436.1:g.9789_9792del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411641.7:c.573+499_573+502del MANE Select	ENSP00000393887.2:n.573+499_573+502del
ENST00000273784.5:c.576+499_576+502del	ENSP00000273784.5:n.576+499_576+502del
ENST00000411641.6:c.573+499_573+502del	ENSP00000393887.2:n.573+499_573+502del
ENST00000478441.1:n.1129_1132del
NM_001622.2:c.573+499_573+502del	NP_001613.2:n.573+499_573+502del
NM_001354571.1:c.576+499_576+502del	NP_001341500.1:n.576+499_576+502del
NM_001354572.1:c.570+499_570+502del	NP_001341501.1:n.570+499_570+502del
NM_001354573.1:c.573+499_573+502del	NP_001341502.1:n.573+499_573+502del
NM_001622.3:c.573+499_573+502del	NP_001613.2:n.573+499_573+502del
NM_001622.4:c.573+499_573+502del MANE Select	NP_001613.2:n.573+499_573+502del
NM_001354571.2:c.576+499_576+502del	NP_001341500.1:n.576+499_576+502del
NM_001354572.2:c.570+499_570+502del	NP_001341501.1:n.570+499_570+502del
NM_001354573.2:c.573+499_573+502del	NP_001341502.1:n.573+499_573+502del