Canonical Allele Identifier: CA5574394
Gene: SFTPA1 HGNC NCBI

Linked Data

dbSNP Id: rs200941736

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.79611960C>A , CM000672.2:g.79611960C>A GRCh38
NC_000010.10:g.81371716C>A , CM000672.1:g.81371716C>A GRCh37
NG_021189.1:g.6022C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000398636.8:c.135C>A MANE Select ENSP00000381633.3:p.Asp45Glu
ENST00000398636.7:c.135C>A ENSP00000381633.3:p.Asp45Glu
ENST00000419470.6:c.180C>A ENSP00000397082.2:p.Asp60Glu
ENST00000428376.6:c.135C>A ENSP00000411102.2:p.Asp45Glu
ENST00000429958.5:c.135C>A ENSP00000395527.1:p.Asp45Glu
ENST00000439264.1:c.135C>A ENSP00000401649.1:p.Asp45Glu
NM_001093770.2:c.180C>A NP_001087239.2:p.Asp60Glu
NM_001164644.1:c.135C>A NP_001158116.1:p.Asp45Glu
NM_001164645.1:c.130+50C>A NP_001158117.1:n.130+50C>A
NM_001164646.1:c.85+50C>A NP_001158118.1:n.85+50C>A
NM_001164647.1:c.135C>A NP_001158119.1:p.Asp45Glu
NM_005411.4:c.135C>A NP_005402.3:p.Asp45Glu
XM_005270062.3:c.135C>A XP_005270119.1:p.Asp45Glu
XM_006717953.2:c.180C>A XP_006718016.1:p.Asp60Glu
XM_005270062.5:c.135C>A XP_005270119.1:p.Asp45Glu
NM_001093770.3:c.180C>A NP_001087239.2:p.Asp60Glu
NM_001164644.2:c.135C>A NP_001158116.1:p.Asp45Glu
NM_001164645.2:c.130+50C>A NP_001158117.1:n.130+50C>A
NM_001164646.2:c.85+50C>A NP_001158118.1:n.85+50C>A
NM_005411.5:c.135C>A MANE Select NP_005402.3:p.Asp45Glu