Canonical Allele Identifier: CA1427019578
Gene: AHSG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.186620638C= , CM000665.2:g.186620638C= GRCh38
NC_000003.11:g.186338427C= , CM000665.1:g.186338427C= GRCh37
NC_000003.10:g.187821121C= NCBI36
NG_011436.1:g.12578C=

Transcript Alleles

HGVS Amino-acid change
ENST00000411641.7:c.812C= MANE Select ENSP00000393887.2:p.Pro271=
ENST00000273784.5:c.815C= ENSP00000273784.5:p.Pro272=
ENST00000411641.6:c.812C= ENSP00000393887.2:p.Pro271=
NM_001622.2:c.812C= NP_001613.2:p.Pro271=
NM_001354571.1:c.815C= NP_001341500.1:p.Pro272=
NM_001354572.1:c.809C= NP_001341501.1:p.Pro270=
NM_001354573.1:c.728C= NP_001341502.1:p.Pro243=
NM_001622.3:c.812C= NP_001613.2:p.Pro271=
NM_001622.4:c.812C= MANE Select NP_001613.2:p.Pro271=
NM_001354571.2:c.815C= NP_001341500.1:p.Pro272=
NM_001354572.2:c.809C= NP_001341501.1:p.Pro270=
NM_001354573.2:c.728C= NP_001341502.1:p.Pro243=