Canonical Allele Identifier: CA1955524021

Gene: SAA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269902A= , CM000673.2:g.18269902A=	GRCh38
NC_000011.9:g.18291449A= , CM000673.1:g.18291449A=	GRCh37
NC_000011.8:g.18248025A=	NCBI36
NG_021330.1:g.8642A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*565A=	ENSP00000509190.1:n.*565A=
ENST00000356524.9:c.*47A= MANE Select	ENSP00000348918.4:n.*47A=
ENST00000649195.1:c.*213A=	ENSP00000497498.1:n.*213A=
ENST00000356524.8:c.*47A=	ENSP00000348918.4:n.*47A=
ENST00000405158.2:c.*47A=	ENSP00000384906.2:n.*47A=
ENST00000532858.5:c.*47A=	ENSP00000436866.1:n.*47A=
NM_000331.4:c.*47A=	NP_000322.2:n.*47A=
NM_001178006.1:c.*47A=	NP_001171477.1:n.*47A=
NM_199161.3:c.*47A=	NP_954630.1:n.*47A=
NM_000331.5:c.*47A=	NP_000322.2:n.*47A=
NM_001178006.2:c.*47A=	NP_001171477.1:n.*47A=
NM_199161.4:c.*47A=	NP_954630.1:n.*47A=
NM_199161.5:c.*47A= MANE Select	NP_954630.2:n.*47A=
NM_000331.6:c.*47A=	NP_000322.3:n.*47A=
NM_001178006.3:c.*47A=	NP_001171477.2:n.*47A=