Canonical Allele Identifier: CA2612728368

Gene: SAA1

Linked Data

• gnomAD v4: 11-18269926-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269926A>G , CM000673.2:g.18269926A>G	GRCh38
NC_000011.9:g.18291473A>G , CM000673.1:g.18291473A>G	GRCh37
NC_000011.8:g.18248049A>G	NCBI36
NG_021330.1:g.8666A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*589A>G	ENSP00000509190.1:n.*589A>G
ENST00000356524.9:c.*71A>G MANE Select	ENSP00000348918.4:n.*71A>G
ENST00000649195.1:c.*237A>G	ENSP00000497498.1:n.*237A>G
ENST00000356524.8:c.*71A>G	ENSP00000348918.4:n.*71A>G
ENST00000405158.2:c.*71A>G	ENSP00000384906.2:n.*71A>G
ENST00000532858.5:c.*71A>G	ENSP00000436866.1:n.*71A>G
NM_000331.4:c.*71A>G	NP_000322.2:n.*71A>G
NM_001178006.1:c.*71A>G	NP_001171477.1:n.*71A>G
NM_199161.3:c.*71A>G	NP_954630.1:n.*71A>G
NM_000331.5:c.*71A>G	NP_000322.2:n.*71A>G
NM_001178006.2:c.*71A>G	NP_001171477.1:n.*71A>G
NM_199161.4:c.*71A>G	NP_954630.1:n.*71A>G
NM_199161.5:c.*71A>G MANE Select	NP_954630.2:n.*71A>G
NM_000331.6:c.*71A>G	NP_000322.3:n.*71A>G
NM_001178006.3:c.*71A>G	NP_001171477.2:n.*71A>G