Canonical Allele Identifier: CA1922240535
Gene: SFTPA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79557186C= , CM000672.2:g.79557186C= GRCh38
NC_000010.10:g.81316942C= , CM000672.1:g.81316942C= GRCh37
NG_013046.1:g.8222G=

Transcript Alleles

HGVS Amino-acid change
ENST00000372325.7:c.*23G= MANE Select ENSP00000361400.2:n.*23G=
ENST00000372325.6:c.*23G= ENSP00000361400.2:n.*23G=
NM_001098668.2:c.*23G= NP_001092138.1:n.*23G=
XM_005270128.2:c.*23G= XP_005270185.1:n.*23G=
XM_005270131.3:c.*23G= XP_005270188.1:n.*23G=
XM_005270132.3:c.*23G= XP_005270189.1:n.*23G=
XM_011540124.1:c.*23G= XP_011538426.1:n.*23G=
XM_011540125.1:c.*23G= XP_011538427.1:n.*23G=
NM_001098668.3:c.*23G= NP_001092138.1:n.*23G=
NM_001320813.1:c.*23G= NP_001307742.1:n.*23G=
NM_001320814.1:c.*23G= NP_001307743.1:n.*23G=
XM_005270128.3:c.*23G= XP_005270185.1:n.*23G=
XM_017016608.1:c.*23G= XP_016872097.1:n.*23G=
NM_001098668.4:c.*23G= MANE Select NP_001092138.1:n.*23G=
NM_001320813.2:c.*23G= NP_001307742.1:n.*23G=