Canonical Allele Identifier: CA2609869157

Gene: SFTPA2

Linked Data

• gnomAD v4: 10-79557544-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79557547_79557549del , CM000672.2:g.79557547_79557549del	GRCh38
NC_000010.10:g.81317303_81317305del , CM000672.1:g.81317303_81317305del	GRCh37
NG_013046.1:g.7861_7863del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372325.7:c.409_411del MANE Select	ENSP00000361400.2:p.Lys137del
ENST00000372325.6:c.409_411del	ENSP00000361400.2:p.Lys137del
ENST00000372327.9:c.409_411del	ENSP00000361402.5:p.Lys137del
ENST00000417041.1:c.409_411del	ENSP00000397375.1:p.Lys137del
NM_001098668.2:c.409_411del	NP_001092138.1:p.Lys137del
XM_005270128.2:c.460_462del	XP_005270185.1:p.Lys154del
XM_005270131.3:c.409_411del	XP_005270188.1:p.Lys137del
XM_005270132.3:c.409_411del	XP_005270189.1:p.Lys137del
XM_011540124.1:c.409_411del	XP_011538426.1:p.Lys137del
XM_011540125.1:c.409_411del	XP_011538427.1:p.Lys137del
NM_001098668.3:c.409_411del	NP_001092138.1:p.Lys137del
NM_001320813.1:c.409_411del	NP_001307742.1:p.Lys137del
NM_001320814.1:c.439_441del	NP_001307743.1:p.Lys147del
XM_005270128.3:c.460_462del	XP_005270185.1:p.Lys154del
XM_017016608.1:c.409_411del	XP_016872097.1:p.Lys137del
NM_001098668.4:c.409_411del MANE Select	NP_001092138.1:p.Lys137del
NM_001320813.2:c.409_411del	NP_001307742.1:p.Lys137del