Canonical Allele Identifier: CA470417533

Gene: SFTPA2

Linked Data

• MyVariant Identifiers: chr10:g.81319132A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79559376A>T , CM000672.2:g.79559376A>T	GRCh38
NC_000010.10:g.81319132A>T , CM000672.1:g.81319132A>T	GRCh37
NG_013046.1:g.6032T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372325.7:c.108T>A MANE Select	ENSP00000361400.2:p.Pro36=
ENST00000372325.6:c.108T>A	ENSP00000361400.2:p.Pro36=
ENST00000372327.9:c.108T>A	ENSP00000361402.5:p.Pro36=
ENST00000417041.1:c.108T>A	ENSP00000397375.1:p.Pro36=
ENST00000492049.1:c.108T>A	ENSP00000473275.1:p.Pro36=
NM_001098668.2:c.108T>A	NP_001092138.1:p.Pro36=
XM_005270128.2:c.159T>A	XP_005270185.1:p.Pro53=
XM_005270131.3:c.108T>A	XP_005270188.1:p.Pro36=
XM_005270132.3:c.108T>A	XP_005270189.1:p.Pro36=
XM_011540124.1:c.108T>A	XP_011538426.1:p.Pro36=
XM_011540125.1:c.108T>A	XP_011538427.1:p.Pro36=
NM_001098668.3:c.108T>A	NP_001092138.1:p.Pro36=
NM_001320813.1:c.108T>A	NP_001307742.1:p.Pro36=
NM_001320814.1:c.138T>A	NP_001307743.1:p.Pro46=
XM_005270128.3:c.159T>A	XP_005270185.1:p.Pro53=
XM_017016608.1:c.108T>A	XP_016872097.1:p.Pro36=
NM_001098668.4:c.108T>A MANE Select	NP_001092138.1:p.Pro36=
NM_001320813.2:c.108T>A	NP_001307742.1:p.Pro36=