Canonical Allele Identifier: CA218566897

Gene: SAA1

Linked Data

• dbSNP Id: rs1044026039
• gnomAD v3: 11-18269965-G-T
• gnomAD v4: 11-18269965-G-T
• MyVariant Identifiers: chr11:g.18291512G>T (hg19) ; chr11:g.18269965G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269965G>T , CM000673.2:g.18269965G>T	GRCh38
NC_000011.9:g.18291512G>T , CM000673.1:g.18291512G>T	GRCh37
NC_000011.8:g.18248088G>T	NCBI36
NG_021330.1:g.8705G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*628G>T	ENSP00000509190.1:n.*628G>T
ENST00000356524.9:c.*110G>T MANE Select	ENSP00000348918.4:n.*110G>T
ENST00000356524.8:c.*110G>T	ENSP00000348918.4:n.*110G>T
ENST00000405158.2:c.*110G>T	ENSP00000384906.2:n.*110G>T
ENST00000532858.5:c.*110G>T	ENSP00000436866.1:n.*110G>T
NM_000331.4:c.*110G>T	NP_000322.2:n.*110G>T
NM_001178006.1:c.*110G>T	NP_001171477.1:n.*110G>T
NM_199161.3:c.*110G>T	NP_954630.1:n.*110G>T
NM_000331.5:c.*110G>T	NP_000322.2:n.*110G>T
NM_001178006.2:c.*110G>T	NP_001171477.1:n.*110G>T
NM_199161.4:c.*110G>T	NP_954630.1:n.*110G>T
NM_199161.5:c.*110G>T MANE Select	NP_954630.2:n.*110G>T
NM_000331.6:c.*110G>T	NP_000322.3:n.*110G>T
NM_001178006.3:c.*110G>T	NP_001171477.2:n.*110G>T