Canonical Allele Identifier: CA674302022

Gene: SAA1

Linked Data

• dbSNP Id: rs1373601924
• gnomAD v3: 11-18269477-G-T
• gnomAD v4: 11-18269477-G-T
• MyVariant Identifiers: chr11:g.18291024G>T (hg19) ; chr11:g.18269477G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269477G>T , CM000673.2:g.18269477G>T	GRCh38
NC_000011.9:g.18291024G>T , CM000673.1:g.18291024G>T	GRCh37
NC_000011.8:g.18247600G>T	NCBI36
NG_021330.1:g.8217G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689650.1:c.*140G>T	ENSP00000509190.1:n.*140G>T
ENST00000356524.9:c.230+144G>T MANE Select	ENSP00000348918.4:n.230+144G>T
ENST00000649195.1:c.*27+113G>T	ENSP00000497498.1:n.*27+113G>T
ENST00000356524.8:c.230+144G>T	ENSP00000348918.4:n.230+144G>T
ENST00000405158.2:c.230+144G>T	ENSP00000384906.2:n.230+144G>T
ENST00000532858.5:c.230+144G>T	ENSP00000436866.1:n.230+144G>T
NM_000331.4:c.230+144G>T	NP_000322.2:n.230+144G>T
NM_001178006.1:c.230+144G>T	NP_001171477.1:n.230+144G>T
NM_199161.3:c.230+144G>T	NP_954630.1:n.230+144G>T
NM_000331.5:c.230+144G>T	NP_000322.2:n.230+144G>T
NM_001178006.2:c.230+144G>T	NP_001171477.1:n.230+144G>T
NM_199161.4:c.230+144G>T	NP_954630.1:n.230+144G>T
NM_199161.5:c.230+144G>T MANE Select	NP_954630.2:n.230+144G>T
NM_000331.6:c.230+144G>T	NP_000322.3:n.230+144G>T
NM_001178006.3:c.230+144G>T	NP_001171477.2:n.230+144G>T