Canonical Allele Identifier: CA5909512

Gene: SAA1

Linked Data

• dbSNP Id: rs747421710
• ExAC: 11:18291222 T / C
• gnomAD v2: 11-18291222-T-C
• gnomAD v4: 11-18269675-T-C
• MyVariant Identifiers: chr11:g.18291222T>C (hg19) ; chr11:g.18269675T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.18269675T>C , CM000673.2:g.18269675T>C	GRCh38
NC_000011.9:g.18291222T>C , CM000673.1:g.18291222T>C	GRCh37
NC_000011.8:g.18247798T>C	NCBI36
NG_021330.1:g.8415T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000689650.1:c.*338T>C	ENSP00000509190.1:n.*338T>C
ENST00000356524.9:c.231-42T>C MANE Select	ENSP00000348918.4:n.231-42T>C
ENST00000649195.1:c.*28-42T>C	ENSP00000497498.1:n.*28-42T>C
ENST00000356524.8:c.231-42T>C	ENSP00000348918.4:n.231-42T>C
ENST00000405158.2:c.231-42T>C	ENSP00000384906.2:n.231-42T>C
ENST00000532858.5:c.231-42T>C	ENSP00000436866.1:n.231-42T>C
NM_000331.4:c.231-42T>C	NP_000322.2:n.231-42T>C
NM_001178006.1:c.231-42T>C	NP_001171477.1:n.231-42T>C
NM_199161.3:c.231-42T>C	NP_954630.1:n.231-42T>C
NM_000331.5:c.231-42T>C	NP_000322.2:n.231-42T>C
NM_001178006.2:c.231-42T>C	NP_001171477.1:n.231-42T>C
NM_199161.4:c.231-42T>C	NP_954630.1:n.231-42T>C
NM_199161.5:c.231-42T>C MANE Select	NP_954630.2:n.231-42T>C
NM_000331.6:c.231-42T>C	NP_000322.3:n.231-42T>C
NM_001178006.3:c.231-42T>C	NP_001171477.2:n.231-42T>C