Canonical Allele Identifier: CA1955523850

Gene: SAA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269540T= , CM000673.2:g.18269540T=	GRCh38
NC_000011.9:g.18291087T= , CM000673.1:g.18291087T=	GRCh37
NC_000011.8:g.18247663T=	NCBI36
NG_021330.1:g.8280T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*203T=	ENSP00000509190.1:n.*203T=
ENST00000356524.9:c.231-177T= MANE Select	ENSP00000348918.4:n.231-177T=
ENST00000649195.1:c.*28-177T=	ENSP00000497498.1:n.*28-177T=
ENST00000356524.8:c.231-177T=	ENSP00000348918.4:n.231-177T=
ENST00000405158.2:c.231-177T=	ENSP00000384906.2:n.231-177T=
ENST00000532858.5:c.231-177T=	ENSP00000436866.1:n.231-177T=
NM_000331.4:c.231-177T=	NP_000322.2:n.231-177T=
NM_001178006.1:c.231-177T=	NP_001171477.1:n.231-177T=
NM_199161.3:c.231-177T=	NP_954630.1:n.231-177T=
NM_000331.5:c.231-177T=	NP_000322.2:n.231-177T=
NM_001178006.2:c.231-177T=	NP_001171477.1:n.231-177T=
NM_199161.4:c.231-177T=	NP_954630.1:n.231-177T=
NM_199161.5:c.231-177T= MANE Select	NP_954630.2:n.231-177T=
NM_000331.6:c.231-177T=	NP_000322.3:n.231-177T=
NM_001178006.3:c.231-177T=	NP_001171477.2:n.231-177T=