Canonical Allele Identifier: CA5573973
Gene: SFTPA2 HGNC NCBI

Linked Data

dbSNP Id: rs759988686

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79557231C>T , CM000672.2:g.79557231C>T GRCh38
NC_000010.10:g.81316987C>T , CM000672.1:g.81316987C>T GRCh37
NG_013046.1:g.8177G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372325.7:c.725G>A MANE Select ENSP00000361400.2:p.Arg242Gln
ENST00000372325.6:c.725G>A ENSP00000361400.2:p.Arg242Gln
ENST00000372327.9:c.725G>A ENSP00000361402.5:p.Arg242Gln
NM_001098668.2:c.725G>A NP_001092138.1:p.Arg242Gln
XM_005270128.2:c.776G>A XP_005270185.1:p.Arg259Gln
XM_005270131.3:c.725G>A XP_005270188.1:p.Arg242Gln
XM_005270132.3:c.725G>A XP_005270189.1:p.Arg242Gln
XM_011540124.1:c.725G>A XP_011538426.1:p.Arg242Gln
XM_011540125.1:c.725G>A XP_011538427.1:p.Arg242Gln
NM_001098668.3:c.725G>A NP_001092138.1:p.Arg242Gln
NM_001320813.1:c.725G>A NP_001307742.1:p.Arg242Gln
NM_001320814.1:c.755G>A NP_001307743.1:p.Arg252Gln
XM_005270128.3:c.776G>A XP_005270185.1:p.Arg259Gln
XM_017016608.1:c.725G>A XP_016872097.1:p.Arg242Gln
NM_001098668.4:c.725G>A MANE Select NP_001092138.1:p.Arg242Gln
NM_001320813.2:c.725G>A NP_001307742.1:p.Arg242Gln