Canonical Allele Identifier: CA1955524044

Gene: SAA1

Linked Data

• dbSNP Id: rs1439491333
• gnomAD v4: 11-18269937-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269937T>A , CM000673.2:g.18269937T>A	GRCh38
NC_000011.9:g.18291484T>A , CM000673.1:g.18291484T>A	GRCh37
NC_000011.8:g.18248060T>A	NCBI36
NG_021330.1:g.8677T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*600T>A	ENSP00000509190.1:n.*600T>A
ENST00000356524.9:c.*82T>A MANE Select	ENSP00000348918.4:n.*82T>A
ENST00000649195.1:c.*248T>A	ENSP00000497498.1:n.*248T>A
ENST00000356524.8:c.*82T>A	ENSP00000348918.4:n.*82T>A
ENST00000405158.2:c.*82T>A	ENSP00000384906.2:n.*82T>A
ENST00000532858.5:c.*82T>A	ENSP00000436866.1:n.*82T>A
NM_000331.4:c.*82T>A	NP_000322.2:n.*82T>A
NM_001178006.1:c.*82T>A	NP_001171477.1:n.*82T>A
NM_199161.3:c.*82T>A	NP_954630.1:n.*82T>A
NM_000331.5:c.*82T>A	NP_000322.2:n.*82T>A
NM_001178006.2:c.*82T>A	NP_001171477.1:n.*82T>A
NM_199161.4:c.*82T>A	NP_954630.1:n.*82T>A
NM_199161.5:c.*82T>A MANE Select	NP_954630.2:n.*82T>A
NM_000331.6:c.*82T>A	NP_000322.3:n.*82T>A
NM_001178006.3:c.*82T>A	NP_001171477.2:n.*82T>A