Canonical Allele Identifier: CA5909540

Gene: SAA1

Linked Data

• dbSNP Id: rs772269963
• ExAC: 11:18291335 A / T
• gnomAD v2: 11-18291335-A-T
• gnomAD v4: 11-18269788-A-T
• MyVariant Identifiers: chr11:g.18291335A>T (hg19) ; chr11:g.18269788A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269788A>T , CM000673.2:g.18269788A>T	GRCh38
NC_000011.9:g.18291335A>T , CM000673.1:g.18291335A>T	GRCh37
NC_000011.8:g.18247911A>T	NCBI36
NG_021330.1:g.8528A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*451A>T	ENSP00000509190.1:n.*451A>T
ENST00000356524.9:c.302A>T MANE Select	ENSP00000348918.4:p.Asn101Ile
ENST00000649195.1:c.*99A>T	ENSP00000497498.1:n.*99A>T
ENST00000356524.8:c.302A>T	ENSP00000348918.4:p.Asn101Ile
ENST00000405158.2:c.302A>T	ENSP00000384906.2:p.Asn101Ile
ENST00000532858.5:c.302A>T	ENSP00000436866.1:p.Asn101Ile
NM_000331.4:c.302A>T	NP_000322.2:p.Asn101Ile
NM_001178006.1:c.302A>T	NP_001171477.1:p.Asn101Ile
NM_199161.3:c.302A>T	NP_954630.1:p.Asn101Ile
NM_000331.5:c.302A>T	NP_000322.2:p.Asn101Ile
NM_001178006.2:c.302A>T	NP_001171477.1:p.Asn101Ile
NM_199161.4:c.302A>T	NP_954630.1:p.Asn101Ile
NM_199161.5:c.302A>T MANE Select	NP_954630.2:p.Asn101Ile
NM_000331.6:c.302A>T	NP_000322.3:p.Asn101Ile
NM_001178006.3:c.302A>T	NP_001171477.2:p.Asn101Ile