Canonical Allele Identifier: CA674302607

Gene: SAA1

Linked Data

• dbSNP Id: rs1195121082
• MyVariant Identifiers: chr11:g.18291493del (hg19) ; chr11:g.18269946del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269947del , CM000673.2:g.18269947del	GRCh38
NC_000011.9:g.18291494del , CM000673.1:g.18291494del	GRCh37
NC_000011.8:g.18248070del	NCBI36
NG_021330.1:g.8687del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*610del	ENSP00000509190.1:n.*610del
ENST00000356524.9:c.*92del MANE Select	ENSP00000348918.4:n.*92del
ENST00000649195.1:c.*258del	ENSP00000497498.1:n.*258del
ENST00000356524.8:c.*92del	ENSP00000348918.4:n.*92del
ENST00000405158.2:c.*92del	ENSP00000384906.2:n.*92del
ENST00000532858.5:c.*92del	ENSP00000436866.1:n.*92del
NM_000331.4:c.*92del	NP_000322.2:n.*92del
NM_001178006.1:c.*92del	NP_001171477.1:n.*92del
NM_199161.3:c.*92del	NP_954630.1:n.*92del
NM_000331.5:c.*92del	NP_000322.2:n.*92del
NM_001178006.2:c.*92del	NP_001171477.1:n.*92del
NM_199161.4:c.*92del	NP_954630.1:n.*92del
NM_199161.5:c.*92del MANE Select	NP_954630.2:n.*92del
NM_000331.6:c.*92del	NP_000322.3:n.*92del
NM_001178006.3:c.*92del	NP_001171477.2:n.*92del