Canonical Allele Identifier: CA2609869178

Gene: SFTPA2

Linked Data

• gnomAD v4: 10-79557598-GAGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79557599_79557601del , CM000672.2:g.79557599_79557601del	GRCh38
NC_000010.10:g.81317355_81317357del , CM000672.1:g.81317355_81317357del	GRCh37
NG_013046.1:g.7807_7809del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372325.7:c.371-16_371-14del MANE Select	ENSP00000361400.2:n.371-16_371-14del
ENST00000372325.6:c.371-16_371-14del	ENSP00000361400.2:n.371-16_371-14del
ENST00000372327.9:c.371-16_371-14del	ENSP00000361402.5:n.371-16_371-14del
ENST00000417041.1:c.371-16_371-14del	ENSP00000397375.1:n.371-16_371-14del
NM_001098668.2:c.371-16_371-14del	NP_001092138.1:n.371-16_371-14del
XM_005270128.2:c.422-16_422-14del	XP_005270185.1:n.422-16_422-14del
XM_005270131.3:c.371-16_371-14del	XP_005270188.1:n.371-16_371-14del
XM_005270132.3:c.371-16_371-14del	XP_005270189.1:n.371-16_371-14del
XM_011540124.1:c.371-16_371-14del	XP_011538426.1:n.371-16_371-14del
XM_011540125.1:c.371-16_371-14del	XP_011538427.1:n.371-16_371-14del
NM_001098668.3:c.371-16_371-14del	NP_001092138.1:n.371-16_371-14del
NM_001320813.1:c.371-16_371-14del	NP_001307742.1:n.371-16_371-14del
NM_001320814.1:c.401-16_401-14del	NP_001307743.1:n.401-16_401-14del
XM_005270128.3:c.422-16_422-14del	XP_005270185.1:n.422-16_422-14del
XM_017016608.1:c.371-16_371-14del	XP_016872097.1:n.371-16_371-14del
NM_001098668.4:c.371-16_371-14del MANE Select	NP_001092138.1:n.371-16_371-14del
NM_001320813.2:c.371-16_371-14del	NP_001307742.1:n.371-16_371-14del