Canonical Allele Identifier: CA1955523947

Gene: SAA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269747T= , CM000673.2:g.18269747T=	GRCh38
NC_000011.9:g.18291294T= , CM000673.1:g.18291294T=	GRCh37
NC_000011.8:g.18247870T=	NCBI36
NG_021330.1:g.8487T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*410T=	ENSP00000509190.1:n.*410T=
ENST00000356524.9:c.261T= MANE Select	ENSP00000348918.4:p.Phe87=
ENST00000649195.1:c.*58T=	ENSP00000497498.1:n.*58T=
ENST00000356524.8:c.261T=	ENSP00000348918.4:p.Phe87=
ENST00000405158.2:c.261T=	ENSP00000384906.2:p.Phe87=
ENST00000532858.5:c.261T=	ENSP00000436866.1:p.Phe87=
NM_000331.4:c.261T=	NP_000322.2:p.Phe87=
NM_001178006.1:c.261T=	NP_001171477.1:p.Phe87=
NM_199161.3:c.261T=	NP_954630.1:p.Phe87=
NM_000331.5:c.261T=	NP_000322.2:p.Phe87=
NM_001178006.2:c.261T=	NP_001171477.1:p.Phe87=
NM_199161.4:c.261T=	NP_954630.1:p.Phe87=
NM_199161.5:c.261T= MANE Select	NP_954630.2:p.Phe87=
NM_000331.6:c.261T=	NP_000322.3:p.Phe87=
NM_001178006.3:c.261T=	NP_001171477.2:p.Phe87=