Canonical Allele Identifier: CA5573959
Gene: SFTPA2 HGNC NCBI

Linked Data

dbSNP Id: rs755871005

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79557175C>G , CM000672.2:g.79557175C>G GRCh38
NC_000010.10:g.81316931C>G , CM000672.1:g.81316931C>G GRCh37
NG_013046.1:g.8233G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000372325.7:c.*34G>C MANE Select ENSP00000361400.2:n.*34G>C
ENST00000372325.6:c.*34G>C ENSP00000361400.2:n.*34G>C
NM_001098668.2:c.*34G>C NP_001092138.1:n.*34G>C
XM_005270128.2:c.*34G>C XP_005270185.1:n.*34G>C
XM_005270131.3:c.*34G>C XP_005270188.1:n.*34G>C
XM_005270132.3:c.*34G>C XP_005270189.1:n.*34G>C
XM_011540124.1:c.*34G>C XP_011538426.1:n.*34G>C
XM_011540125.1:c.*34G>C XP_011538427.1:n.*34G>C
NM_001098668.3:c.*34G>C NP_001092138.1:n.*34G>C
NM_001320813.1:c.*34G>C NP_001307742.1:n.*34G>C
NM_001320814.1:c.*34G>C NP_001307743.1:n.*34G>C
XM_005270128.3:c.*34G>C XP_005270185.1:n.*34G>C
XM_017016608.1:c.*34G>C XP_016872097.1:n.*34G>C
NM_001098668.4:c.*34G>C MANE Select NP_001092138.1:n.*34G>C
NM_001320813.2:c.*34G>C NP_001307742.1:n.*34G>C