Canonical Allele Identifier: CA597451560

Gene: SAA1

Linked Data

• dbSNP Id: rs1229041336
• gnomAD v2: 11-18291508-G-A
• gnomAD v3: 11-18269961-G-A
• gnomAD v4: 11-18269961-G-A
• MyVariant Identifiers: chr11:g.18291508G>A (hg19) ; chr11:g.18269961G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269961G>A , CM000673.2:g.18269961G>A	GRCh38
NC_000011.9:g.18291508G>A , CM000673.1:g.18291508G>A	GRCh37
NC_000011.8:g.18248084G>A	NCBI36
NG_021330.1:g.8701G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*624G>A	ENSP00000509190.1:n.*624G>A
ENST00000356524.9:c.*106G>A MANE Select	ENSP00000348918.4:n.*106G>A
ENST00000649195.1:c.*272G>A	ENSP00000497498.1:n.*272G>A
ENST00000356524.8:c.*106G>A	ENSP00000348918.4:n.*106G>A
ENST00000405158.2:c.*106G>A	ENSP00000384906.2:n.*106G>A
ENST00000532858.5:c.*106G>A	ENSP00000436866.1:n.*106G>A
NM_000331.4:c.*106G>A	NP_000322.2:n.*106G>A
NM_001178006.1:c.*106G>A	NP_001171477.1:n.*106G>A
NM_199161.3:c.*106G>A	NP_954630.1:n.*106G>A
NM_000331.5:c.*106G>A	NP_000322.2:n.*106G>A
NM_001178006.2:c.*106G>A	NP_001171477.1:n.*106G>A
NM_199161.4:c.*106G>A	NP_954630.1:n.*106G>A
NM_199161.5:c.*106G>A MANE Select	NP_954630.2:n.*106G>A
NM_000331.6:c.*106G>A	NP_000322.3:n.*106G>A
NM_001178006.3:c.*106G>A	NP_001171477.2:n.*106G>A