Canonical Allele Identifier: CA2612727504
Gene: SAA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18269453C>T , CM000673.2:g.18269453C>T GRCh38
NC_000011.9:g.18291000C>T , CM000673.1:g.18291000C>T GRCh37
NC_000011.8:g.18247576C>T NCBI36
NG_021330.1:g.8193C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000689650.1:c.*116C>T ENSP00000509190.1:n.*116C>T
ENST00000356524.9:c.230+120C>T MANE Select ENSP00000348918.4:n.230+120C>T
ENST00000649195.1:c.*27+89C>T ENSP00000497498.1:n.*27+89C>T
ENST00000356524.8:c.230+120C>T ENSP00000348918.4:n.230+120C>T
ENST00000405158.2:c.230+120C>T ENSP00000384906.2:n.230+120C>T
ENST00000532858.5:c.230+120C>T ENSP00000436866.1:n.230+120C>T
NM_000331.4:c.230+120C>T NP_000322.2:n.230+120C>T
NM_001178006.1:c.230+120C>T NP_001171477.1:n.230+120C>T
NM_199161.3:c.230+120C>T NP_954630.1:n.230+120C>T
NM_000331.5:c.230+120C>T NP_000322.2:n.230+120C>T
NM_001178006.2:c.230+120C>T NP_001171477.1:n.230+120C>T
NM_199161.4:c.230+120C>T NP_954630.1:n.230+120C>T
NM_199161.5:c.230+120C>T MANE Select NP_954630.2:n.230+120C>T
NM_000331.6:c.230+120C>T NP_000322.3:n.230+120C>T
NM_001178006.3:c.230+120C>T NP_001171477.2:n.230+120C>T