Canonical Allele Identifier: CA379505782
Gene: SAA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18269739A>G , CM000673.2:g.18269739A>G GRCh38
NC_000011.9:g.18291286A>G , CM000673.1:g.18291286A>G GRCh37
NC_000011.8:g.18247862A>G NCBI36
NG_021330.1:g.8479A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689650.1:c.*402A>G ENSP00000509190.1:n.*402A>G
ENST00000356524.9:c.253A>G MANE Select ENSP00000348918.4:p.Arg85Gly
ENST00000649195.1:c.*50A>G ENSP00000497498.1:n.*50A>G
ENST00000356524.8:c.253A>G ENSP00000348918.4:p.Arg85Gly
ENST00000405158.2:c.253A>G ENSP00000384906.2:p.Arg85Gly
ENST00000532858.5:c.253A>G ENSP00000436866.1:p.Arg85Gly
NM_000331.4:c.253A>G NP_000322.2:p.Arg85Gly
NM_001178006.1:c.253A>G NP_001171477.1:p.Arg85Gly
NM_199161.3:c.253A>G NP_954630.1:p.Arg85Gly
NM_000331.5:c.253A>G NP_000322.2:p.Arg85Gly
NM_001178006.2:c.253A>G NP_001171477.1:p.Arg85Gly
NM_199161.4:c.253A>G NP_954630.1:p.Arg85Gly
NM_199161.5:c.253A>G MANE Select NP_954630.2:p.Arg85Gly
NM_000331.6:c.253A>G NP_000322.3:p.Arg85Gly
NM_001178006.3:c.253A>G NP_001171477.2:p.Arg85Gly