Canonical Allele Identifier: CA935588815

Gene: SAA1

Linked Data

• dbSNP Id: rs1858160037
• gnomAD v3: 11-18269668-TG-T
• gnomAD v4: 11-18269668-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269669del , CM000673.2:g.18269669del	GRCh38
NC_000011.9:g.18291216del , CM000673.1:g.18291216del	GRCh37
NC_000011.8:g.18247792del	NCBI36
NG_021330.1:g.8409del

Transcript Alleles

HGVS	Amino-acid change
ENST00000689650.1:c.*332del	ENSP00000509190.1:n.*332del
ENST00000356524.9:c.231-48del MANE Select	ENSP00000348918.4:n.231-48del
ENST00000649195.1:c.*28-48del	ENSP00000497498.1:n.*28-48del
ENST00000356524.8:c.231-48del	ENSP00000348918.4:n.231-48del
ENST00000405158.2:c.231-48del	ENSP00000384906.2:n.231-48del
ENST00000532858.5:c.231-48del	ENSP00000436866.1:n.231-48del
NM_000331.4:c.231-48del	NP_000322.2:n.231-48del
NM_001178006.1:c.231-48del	NP_001171477.1:n.231-48del
NM_199161.3:c.231-48del	NP_954630.1:n.231-48del
NM_000331.5:c.231-48del	NP_000322.2:n.231-48del
NM_001178006.2:c.231-48del	NP_001171477.1:n.231-48del
NM_199161.4:c.231-48del	NP_954630.1:n.231-48del
NM_199161.5:c.231-48del MANE Select	NP_954630.2:n.231-48del
NM_000331.6:c.231-48del	NP_000322.3:n.231-48del
NM_001178006.3:c.231-48del	NP_001171477.2:n.231-48del