Canonical Allele Identifier: CA1427019579
Gene: AHSG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186620639C= , CM000665.2:g.186620639C= GRCh38
NC_000003.11:g.186338428C= , CM000665.1:g.186338428C= GRCh37
NC_000003.10:g.187821122C= NCBI36
NG_011436.1:g.12579C=

Transcript Alleles

HGVS Amino-acid change
ENST00000411641.7:c.813C= MANE Select ENSP00000393887.2:p.Pro271=
ENST00000273784.5:c.816C= ENSP00000273784.5:p.Pro272=
ENST00000411641.6:c.813C= ENSP00000393887.2:p.Pro271=
NM_001622.2:c.813C= NP_001613.2:p.Pro271=
NM_001354571.1:c.816C= NP_001341500.1:p.Pro272=
NM_001354572.1:c.810C= NP_001341501.1:p.Pro270=
NM_001354573.1:c.729C= NP_001341502.1:p.Pro243=
NM_001622.3:c.813C= NP_001613.2:p.Pro271=
NM_001622.4:c.813C= MANE Select NP_001613.2:p.Pro271=
NM_001354571.2:c.816C= NP_001341500.1:p.Pro272=
NM_001354572.2:c.810C= NP_001341501.1:p.Pro270=
NM_001354573.2:c.729C= NP_001341502.1:p.Pro243=