Canonical Allele Identifier: CA2612728342

Gene: SAA1

Linked Data

• gnomAD v4: 11-18269897-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269897C>A , CM000673.2:g.18269897C>A	GRCh38
NC_000011.9:g.18291444C>A , CM000673.1:g.18291444C>A	GRCh37
NC_000011.8:g.18248020C>A	NCBI36
NG_021330.1:g.8637C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*560C>A	ENSP00000509190.1:n.*560C>A
ENST00000356524.9:c.*42C>A MANE Select	ENSP00000348918.4:n.*42C>A
ENST00000649195.1:c.*208C>A	ENSP00000497498.1:n.*208C>A
ENST00000356524.8:c.*42C>A	ENSP00000348918.4:n.*42C>A
ENST00000405158.2:c.*42C>A	ENSP00000384906.2:n.*42C>A
ENST00000532858.5:c.*42C>A	ENSP00000436866.1:n.*42C>A
NM_000331.4:c.*42C>A	NP_000322.2:n.*42C>A
NM_001178006.1:c.*42C>A	NP_001171477.1:n.*42C>A
NM_199161.3:c.*42C>A	NP_954630.1:n.*42C>A
NM_000331.5:c.*42C>A	NP_000322.2:n.*42C>A
NM_001178006.2:c.*42C>A	NP_001171477.1:n.*42C>A
NM_199161.4:c.*42C>A	NP_954630.1:n.*42C>A
NM_199161.5:c.*42C>A MANE Select	NP_954630.2:n.*42C>A
NM_000331.6:c.*42C>A	NP_000322.3:n.*42C>A
NM_001178006.3:c.*42C>A	NP_001171477.2:n.*42C>A