Canonical Allele Identifier: CA1922240896
Gene: SFTPA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79557415_79557418delinsACTT , CM000672.2:g.79557415_79557418delinsACTT GRCh38
NC_000010.10:g.81317171_81317174delinsACTT , CM000672.1:g.81317171_81317174delinsACTT GRCh37
NG_013046.1:g.7990_7993delinsAAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000372325.7:c.538_541delinsAAGT MANE Select ENSP00000361400.2:p.Lys180=
ENST00000372325.6:c.538_541delinsAAGT ENSP00000361400.2:p.Lys180=
ENST00000372327.9:c.538_541delinsAAGT ENSP00000361402.5:p.Lys180=
NM_001098668.2:c.538_541delinsAAGT NP_001092138.1:p.Lys180=
XM_005270128.2:c.589_592delinsAAGT XP_005270185.1:p.Lys197=
XM_005270131.3:c.538_541delinsAAGT XP_005270188.1:p.Lys180=
XM_005270132.3:c.538_541delinsAAGT XP_005270189.1:p.Lys180=
XM_011540124.1:c.538_541delinsAAGT XP_011538426.1:p.Lys180=
XM_011540125.1:c.538_541delinsAAGT XP_011538427.1:p.Lys180=
NM_001098668.3:c.538_541delinsAAGT NP_001092138.1:p.Lys180=
NM_001320813.1:c.538_541delinsAAGT NP_001307742.1:p.Lys180=
NM_001320814.1:c.568_571delinsAAGT NP_001307743.1:p.Lys190=
XM_005270128.3:c.589_592delinsAAGT XP_005270185.1:p.Lys197=
XM_017016608.1:c.538_541delinsAAGT XP_016872097.1:p.Lys180=
NM_001098668.4:c.538_541delinsAAGT MANE Select NP_001092138.1:p.Lys180=
NM_001320813.2:c.538_541delinsAAGT NP_001307742.1:p.Lys180=