Canonical Allele Identifier: CA1955523761

Gene: SAA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269355_18269356delinsTT , CM000673.2:g.18269355_18269356delinsTT	GRCh38
NC_000011.9:g.18290902_18290903delinsTT , CM000673.1:g.18290902_18290903delinsTT	GRCh37
NC_000011.8:g.18247478_18247479delinsTT	NCBI36
NG_021330.1:g.8095_8096delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*18_*19delinsTT	ENSP00000509190.1:n.*18_*19delinsTT
ENST00000356524.9:c.230+22_230+23delinsTT MANE Select	ENSP00000348918.4:n.230+22_230+23delinsTT
ENST00000649195.1:c.*18_*19delinsTT	ENSP00000497498.1:n.*18_*19delinsTT
ENST00000356524.8:c.230+22_230+23delinsTT	ENSP00000348918.4:n.230+22_230+23delinsTT
ENST00000405158.2:c.230+22_230+23delinsTT	ENSP00000384906.2:n.230+22_230+23delinsTT
ENST00000532858.5:c.230+22_230+23delinsTT	ENSP00000436866.1:n.230+22_230+23delinsTT
NM_000331.4:c.230+22_230+23delinsTT	NP_000322.2:n.230+22_230+23delinsTT
NM_001178006.1:c.230+22_230+23delinsTT	NP_001171477.1:n.230+22_230+23delinsTT
NM_199161.3:c.230+22_230+23delinsTT	NP_954630.1:n.230+22_230+23delinsTT
NM_000331.5:c.230+22_230+23delinsTT	NP_000322.2:n.230+22_230+23delinsTT
NM_001178006.2:c.230+22_230+23delinsTT	NP_001171477.1:n.230+22_230+23delinsTT
NM_199161.4:c.230+22_230+23delinsTT	NP_954630.1:n.230+22_230+23delinsTT
NM_199161.5:c.230+22_230+23delinsTT MANE Select	NP_954630.2:n.230+22_230+23delinsTT
NM_000331.6:c.230+22_230+23delinsTT	NP_000322.3:n.230+22_230+23delinsTT
NM_001178006.3:c.230+22_230+23delinsTT	NP_001171477.2:n.230+22_230+23delinsTT