Canonical Allele Identifier: CA653600363
Gene: SFTPA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79557057_79557058insA , CM000672.2:g.79557057_79557058insA GRCh38
NC_000010.10:g.81316813_81316814insA , CM000672.1:g.81316813_81316814insA GRCh37
NG_013046.1:g.8350_8351insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372325.7:c.*151_*152insT MANE Select ENSP00000361400.2:n.*151_*152insT
ENST00000372325.6:c.*151_*152insT ENSP00000361400.2:n.*151_*152insT
NM_001098668.2:c.*151_*152insT NP_001092138.1:n.*151_*152insT
XM_005270128.2:c.*151_*152insT XP_005270185.1:n.*151_*152insT
XM_005270131.3:c.*151_*152insT XP_005270188.1:n.*151_*152insT
XM_005270132.3:c.*151_*152insT XP_005270189.1:n.*151_*152insT
XM_011540124.1:c.*151_*152insT XP_011538426.1:n.*151_*152insT
XM_011540125.1:c.*151_*152insT XP_011538427.1:n.*151_*152insT
NM_001098668.3:c.*151_*152insT NP_001092138.1:n.*151_*152insT
NM_001320813.1:c.*151_*152insT NP_001307742.1:n.*151_*152insT
NM_001320814.1:c.*151_*152insT NP_001307743.1:n.*151_*152insT
XM_005270128.3:c.*151_*152insT XP_005270185.1:n.*151_*152insT
XM_017016608.1:c.*151_*152insT XP_016872097.1:n.*151_*152insT
NM_001098668.4:c.*151_*152insT MANE Select NP_001092138.1:n.*151_*152insT
NM_001320813.2:c.*151_*152insT NP_001307742.1:n.*151_*152insT