Canonical Allele Identifier: CA1955523995

Gene: SAA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269840G= , CM000673.2:g.18269840G=	GRCh38
NC_000011.9:g.18291387G= , CM000673.1:g.18291387G=	GRCh37
NC_000011.8:g.18247963G=	NCBI36
NG_021330.1:g.8580G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*503G=	ENSP00000509190.1:n.*503G=
ENST00000356524.9:c.354G= MANE Select	ENSP00000348918.4:p.Leu118=
ENST00000649195.1:c.*151G=	ENSP00000497498.1:n.*151G=
ENST00000356524.8:c.354G=	ENSP00000348918.4:p.Leu118=
ENST00000405158.2:c.354G=	ENSP00000384906.2:p.Leu118=
ENST00000532858.5:c.354G=	ENSP00000436866.1:p.Leu118=
NM_000331.4:c.354G=	NP_000322.2:p.Leu118=
NM_001178006.1:c.354G=	NP_001171477.1:p.Leu118=
NM_199161.3:c.354G=	NP_954630.1:p.Leu118=
NM_000331.5:c.354G=	NP_000322.2:p.Leu118=
NM_001178006.2:c.354G=	NP_001171477.1:p.Leu118=
NM_199161.4:c.354G=	NP_954630.1:p.Leu118=
NM_199161.5:c.354G= MANE Select	NP_954630.2:p.Leu118=
NM_000331.6:c.354G=	NP_000322.3:p.Leu118=
NM_001178006.3:c.354G=	NP_001171477.2:p.Leu118=