Canonical Allele Identifier: CA379506278
Gene: SAA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18269793T>A , CM000673.2:g.18269793T>A GRCh38
NC_000011.9:g.18291340T>A , CM000673.1:g.18291340T>A GRCh37
NC_000011.8:g.18247916T>A NCBI36
NG_021330.1:g.8533T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000689650.1:c.*456T>A ENSP00000509190.1:n.*456T>A
ENST00000356524.9:c.307T>A MANE Select ENSP00000348918.4:p.Trp103Arg
ENST00000649195.1:c.*104T>A ENSP00000497498.1:n.*104T>A
ENST00000356524.8:c.307T>A ENSP00000348918.4:p.Trp103Arg
ENST00000405158.2:c.307T>A ENSP00000384906.2:p.Trp103Arg
ENST00000532858.5:c.307T>A ENSP00000436866.1:p.Trp103Arg
NM_000331.4:c.307T>A NP_000322.2:p.Trp103Arg
NM_001178006.1:c.307T>A NP_001171477.1:p.Trp103Arg
NM_199161.3:c.307T>A NP_954630.1:p.Trp103Arg
NM_000331.5:c.307T>A NP_000322.2:p.Trp103Arg
NM_001178006.2:c.307T>A NP_001171477.1:p.Trp103Arg
NM_199161.4:c.307T>A NP_954630.1:p.Trp103Arg
NM_199161.5:c.307T>A MANE Select NP_954630.2:p.Trp103Arg
NM_000331.6:c.307T>A NP_000322.3:p.Trp103Arg
NM_001178006.3:c.307T>A NP_001171477.2:p.Trp103Arg