Canonical Allele Identifier: CA1922245573

Gene: SFTPA2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79559458G= , CM000672.2:g.79559458G=	GRCh38
NC_000010.10:g.81319214G= , CM000672.1:g.81319214G=	GRCh37
NG_013046.1:g.5950C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372325.7:c.26C= MANE Select	ENSP00000361400.2:p.Thr9=
ENST00000640627.1:c.71C=	ENSP00000492537.1:p.Thr24=
ENST00000372325.6:c.26C=	ENSP00000361400.2:p.Thr9=
ENST00000372327.9:c.26C=	ENSP00000361402.5:p.Thr9=
ENST00000417041.1:c.26C=	ENSP00000397375.1:p.Thr9=
ENST00000492049.1:c.26C=	ENSP00000473275.1:p.Thr9=
NM_001098668.2:c.26C=	NP_001092138.1:p.Thr9=
XM_005270128.2:c.77C=	XP_005270185.1:p.Thr26=
XM_005270131.3:c.26C=	XP_005270188.1:p.Thr9=
XM_005270132.3:c.26C=	XP_005270189.1:p.Thr9=
XM_011540124.1:c.26C=	XP_011538426.1:p.Thr9=
XM_011540125.1:c.26C=	XP_011538427.1:p.Thr9=
NM_001098668.3:c.26C=	NP_001092138.1:p.Thr9=
NM_001320813.1:c.26C=	NP_001307742.1:p.Thr9=
NM_001320814.1:c.56C=	NP_001307743.1:p.Thr19=
XM_005270128.3:c.77C=	XP_005270185.1:p.Thr26=
XM_017016608.1:c.26C=	XP_016872097.1:p.Thr9=
NM_001098668.4:c.26C= MANE Select	NP_001092138.1:p.Thr9=
NM_001320813.2:c.26C=	NP_001307742.1:p.Thr9=