Canonical Allele Identifier: CA1427018597
Gene: AHSG HGNC NCBI

Linked Data

dbSNP Id: rs1716371939
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186618313del , CM000665.2:g.186618313del GRCh38
NC_000003.11:g.186336102del , CM000665.1:g.186336102del GRCh37
NC_000003.10:g.187818796del NCBI36
NG_011436.1:g.10253del

Transcript Alleles

HGVS Amino-acid change
ENST00000411641.7:c.574-223del MANE Select ENSP00000393887.2:n.574-223del
ENST00000273784.5:c.577-223del ENSP00000273784.5:n.577-223del
ENST00000411641.6:c.574-223del ENSP00000393887.2:n.574-223del
NM_001622.2:c.574-223del NP_001613.2:n.574-223del
NM_001354571.1:c.577-223del NP_001341500.1:n.577-223del
NM_001354572.1:c.571-223del NP_001341501.1:n.571-223del
NM_001354573.1:c.574-223del NP_001341502.1:n.574-223del
NM_001622.3:c.574-223del NP_001613.2:n.574-223del
NM_001622.4:c.574-223del MANE Select NP_001613.2:n.574-223del
NM_001354571.2:c.577-223del NP_001341500.1:n.577-223del
NM_001354572.2:c.571-223del NP_001341501.1:n.571-223del
NM_001354573.2:c.574-223del NP_001341502.1:n.574-223del
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