Canonical Allele Identifier: CA1955524041

Gene: SAA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269934C= , CM000673.2:g.18269934C=	GRCh38
NC_000011.9:g.18291481C= , CM000673.1:g.18291481C=	GRCh37
NC_000011.8:g.18248057C=	NCBI36
NG_021330.1:g.8674C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*597C=	ENSP00000509190.1:n.*597C=
ENST00000356524.9:c.*79C= MANE Select	ENSP00000348918.4:n.*79C=
ENST00000649195.1:c.*245C=	ENSP00000497498.1:n.*245C=
ENST00000356524.8:c.*79C=	ENSP00000348918.4:n.*79C=
ENST00000405158.2:c.*79C=	ENSP00000384906.2:n.*79C=
ENST00000532858.5:c.*79C=	ENSP00000436866.1:n.*79C=
NM_000331.4:c.*79C=	NP_000322.2:n.*79C=
NM_001178006.1:c.*79C=	NP_001171477.1:n.*79C=
NM_199161.3:c.*79C=	NP_954630.1:n.*79C=
NM_000331.5:c.*79C=	NP_000322.2:n.*79C=
NM_001178006.2:c.*79C=	NP_001171477.1:n.*79C=
NM_199161.4:c.*79C=	NP_954630.1:n.*79C=
NM_199161.5:c.*79C= MANE Select	NP_954630.2:n.*79C=
NM_000331.6:c.*79C=	NP_000322.3:n.*79C=
NM_001178006.3:c.*79C=	NP_001171477.2:n.*79C=