Canonical Allele Identifier: CA2612727782

Gene: SAA1

Linked Data

• gnomAD v4: 11-18269658-G-GCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269658_18269659insCCT , CM000673.2:g.18269658_18269659insCCT	GRCh38
NC_000011.9:g.18291205_18291206insCCT , CM000673.1:g.18291205_18291206insCCT	GRCh37
NC_000011.8:g.18247781_18247782insCCT	NCBI36
NG_021330.1:g.8398_8399insCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*321_*322insCCT	ENSP00000509190.1:n.*321_*322insCCT
ENST00000356524.9:c.231-59_231-58insCCT MANE Select	ENSP00000348918.4:n.231-59_231-58insCCT
ENST00000649195.1:c.*28-59_*28-58insCCT	ENSP00000497498.1:n.*28-59_*28-58insCCT
ENST00000356524.8:c.231-59_231-58insCCT	ENSP00000348918.4:n.231-59_231-58insCCT
ENST00000405158.2:c.231-59_231-58insCCT	ENSP00000384906.2:n.231-59_231-58insCCT
ENST00000532858.5:c.231-59_231-58insCCT	ENSP00000436866.1:n.231-59_231-58insCCT
NM_000331.4:c.231-59_231-58insCCT	NP_000322.2:n.231-59_231-58insCCT
NM_001178006.1:c.231-59_231-58insCCT	NP_001171477.1:n.231-59_231-58insCCT
NM_199161.3:c.231-59_231-58insCCT	NP_954630.1:n.231-59_231-58insCCT
NM_000331.5:c.231-59_231-58insCCT	NP_000322.2:n.231-59_231-58insCCT
NM_001178006.2:c.231-59_231-58insCCT	NP_001171477.1:n.231-59_231-58insCCT
NM_199161.4:c.231-59_231-58insCCT	NP_954630.1:n.231-59_231-58insCCT
NM_199161.5:c.231-59_231-58insCCT MANE Select	NP_954630.2:n.231-59_231-58insCCT
NM_000331.6:c.231-59_231-58insCCT	NP_000322.3:n.231-59_231-58insCCT
NM_001178006.3:c.231-59_231-58insCCT	NP_001171477.2:n.231-59_231-58insCCT