Canonical Allele Identifier: CA1955523737

Gene: SAA1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269333C= , CM000673.2:g.18269333C=	GRCh38
NC_000011.9:g.18290880C= , CM000673.1:g.18290880C=	GRCh37
NC_000011.8:g.18247456C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.230C=	ENSP00000509190.1:p.Thr77=
ENST00000356524.9:c.230C= MANE Select	ENSP00000348918.4:p.Thr77=
ENST00000649195.1:c.230C=	ENSP00000497498.1:p.Thr77=
ENST00000356524.8:c.230C=	ENSP00000348918.4:p.Thr77=
ENST00000405158.2:c.230C=	ENSP00000384906.2:p.Thr77=
ENST00000532858.5:c.230C=	ENSP00000436866.1:p.Thr77=
NM_199161.5:c.230C= MANE Select	NP_954630.2:p.Thr77=
NM_000331.6:c.230C=	NP_000322.3:p.Thr77=
NM_001178006.3:c.230C=	NP_001171477.2:p.Thr77=