Canonical Allele Identifier: CA1955523808
Gene: SAA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18269438_18269441delinsCCCT , CM000673.2:g.18269438_18269441delinsCCCT GRCh38
NC_000011.9:g.18290985_18290988delinsCCCT , CM000673.1:g.18290985_18290988delinsCCCT GRCh37
NC_000011.8:g.18247561_18247564delinsCCCT NCBI36
NG_021330.1:g.8178_8181delinsCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000689650.1:c.*101_*104delinsCCCT ENSP00000509190.1:n.*101_*104delinsCCCT
ENST00000356524.9:c.230+105_230+108delinsCCCT MANE Select ENSP00000348918.4:n.230+105_230+108delinsCCCT
ENST00000649195.1:c.*27+74_*27+77delinsCCCT ENSP00000497498.1:n.*27+74_*27+77delinsCCCT
ENST00000356524.8:c.230+105_230+108delinsCCCT ENSP00000348918.4:n.230+105_230+108delinsCCCT
ENST00000405158.2:c.230+105_230+108delinsCCCT ENSP00000384906.2:n.230+105_230+108delinsCCCT
ENST00000532858.5:c.230+105_230+108delinsCCCT ENSP00000436866.1:n.230+105_230+108delinsCCCT
NM_000331.4:c.230+105_230+108delinsCCCT NP_000322.2:n.230+105_230+108delinsCCCT
NM_001178006.1:c.230+105_230+108delinsCCCT NP_001171477.1:n.230+105_230+108delinsCCCT
NM_199161.3:c.230+105_230+108delinsCCCT NP_954630.1:n.230+105_230+108delinsCCCT
NM_000331.5:c.230+105_230+108delinsCCCT NP_000322.2:n.230+105_230+108delinsCCCT
NM_001178006.2:c.230+105_230+108delinsCCCT NP_001171477.1:n.230+105_230+108delinsCCCT
NM_199161.4:c.230+105_230+108delinsCCCT NP_954630.1:n.230+105_230+108delinsCCCT
NM_199161.5:c.230+105_230+108delinsCCCT MANE Select NP_954630.2:n.230+105_230+108delinsCCCT
NM_000331.6:c.230+105_230+108delinsCCCT NP_000322.3:n.230+105_230+108delinsCCCT
NM_001178006.3:c.230+105_230+108delinsCCCT NP_001171477.2:n.230+105_230+108delinsCCCT