Canonical Allele Identifier: CA1955524017

Gene: SAA1

Linked Data

• dbSNP Id: rs1858174444

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269895_18269898del , CM000673.2:g.18269895_18269898del	GRCh38
NC_000011.9:g.18291442_18291445del , CM000673.1:g.18291442_18291445del	GRCh37
NC_000011.8:g.18248018_18248021del	NCBI36
NG_021330.1:g.8635_8638del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*558_*561del	ENSP00000509190.1:n.*558_*561del
ENST00000356524.9:c.*40_*43del MANE Select	ENSP00000348918.4:n.*40_*43del
ENST00000649195.1:c.*206_*209del	ENSP00000497498.1:n.*206_*209del
ENST00000356524.8:c.*40_*43del	ENSP00000348918.4:n.*40_*43del
ENST00000405158.2:c.*40_*43del	ENSP00000384906.2:n.*40_*43del
ENST00000532858.5:c.*40_*43del	ENSP00000436866.1:n.*40_*43del
NM_000331.4:c.*40_*43del	NP_000322.2:n.*40_*43del
NM_001178006.1:c.*40_*43del	NP_001171477.1:n.*40_*43del
NM_199161.3:c.*40_*43del	NP_954630.1:n.*40_*43del
NM_000331.5:c.*40_*43del	NP_000322.2:n.*40_*43del
NM_001178006.2:c.*40_*43del	NP_001171477.1:n.*40_*43del
NM_199161.4:c.*40_*43del	NP_954630.1:n.*40_*43del
NM_199161.5:c.*40_*43del MANE Select	NP_954630.2:n.*40_*43del
NM_000331.6:c.*40_*43del	NP_000322.3:n.*40_*43del
NM_001178006.3:c.*40_*43del	NP_001171477.2:n.*40_*43del