Canonical Allele Identifier: CA2574773470
Gene: SAA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18269957_18269958del , CM000673.2:g.18269957_18269958del GRCh38
NC_000011.9:g.18291504_18291505del , CM000673.1:g.18291504_18291505del GRCh37
NC_000011.8:g.18248080_18248081del NCBI36
NG_021330.1:g.8697_8698del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689650.1:c.*620_*621del ENSP00000509190.1:n.*620_*621del
ENST00000356524.9:c.*102_*103del MANE Select ENSP00000348918.4:n.*102_*103del
ENST00000649195.1:c.*268_*269del ENSP00000497498.1:n.*268_*269del
ENST00000356524.8:c.*102_*103del ENSP00000348918.4:n.*102_*103del
ENST00000405158.2:c.*102_*103del ENSP00000384906.2:n.*102_*103del
ENST00000532858.5:c.*102_*103del ENSP00000436866.1:n.*102_*103del
NM_000331.4:c.*102_*103del NP_000322.2:n.*102_*103del
NM_001178006.1:c.*102_*103del NP_001171477.1:n.*102_*103del
NM_199161.3:c.*102_*103del NP_954630.1:n.*102_*103del
NM_000331.5:c.*102_*103del NP_000322.2:n.*102_*103del
NM_001178006.2:c.*102_*103del NP_001171477.1:n.*102_*103del
NM_199161.4:c.*102_*103del NP_954630.1:n.*102_*103del
NM_199161.5:c.*102_*103del MANE Select NP_954630.2:n.*102_*103del
NM_000331.6:c.*102_*103del NP_000322.3:n.*102_*103del
NM_001178006.3:c.*102_*103del NP_001171477.2:n.*102_*103del