Canonical Allele Identifier: CA2612728317

Gene: SAA1

Linked Data

• gnomAD v4: 11-18269857-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269859del , CM000673.2:g.18269859del	GRCh38
NC_000011.9:g.18291406del , CM000673.1:g.18291406del	GRCh37
NC_000011.8:g.18247982del	NCBI36
NG_021330.1:g.8599del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*522del	ENSP00000509190.1:n.*522del
ENST00000356524.9:c.*4del MANE Select	ENSP00000348918.4:n.*4del
ENST00000649195.1:c.*170del	ENSP00000497498.1:n.*170del
ENST00000356524.8:c.*4del	ENSP00000348918.4:n.*4del
ENST00000405158.2:c.*4del	ENSP00000384906.2:n.*4del
ENST00000532858.5:c.*4del	ENSP00000436866.1:n.*4del
NM_000331.4:c.*4del	NP_000322.2:n.*4del
NM_001178006.1:c.*4del	NP_001171477.1:n.*4del
NM_199161.3:c.*4del	NP_954630.1:n.*4del
NM_000331.5:c.*4del	NP_000322.2:n.*4del
NM_001178006.2:c.*4del	NP_001171477.1:n.*4del
NM_199161.4:c.*4del	NP_954630.1:n.*4del
NM_199161.5:c.*4del MANE Select	NP_954630.2:n.*4del
NM_000331.6:c.*4del	NP_000322.3:n.*4del
NM_001178006.3:c.*4del	NP_001171477.2:n.*4del