Canonical Allele Identifier: CA377354332

Gene: SFTPA2

Linked Data

• gnomAD v4: 10-79559444-C-A
• MyVariant Identifiers: chr10:g.81319200C>A (hg19) ; chr10:g.79559444C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79559444C>A , CM000672.2:g.79559444C>A	GRCh38
NC_000010.10:g.81319200C>A , CM000672.1:g.81319200C>A	GRCh37
NG_013046.1:g.5964G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372325.7:c.40G>T MANE Select	ENSP00000361400.2:p.Ala14Ser
ENST00000640627.1:c.85G>T	ENSP00000492537.1:p.Ala29Ser
ENST00000372325.6:c.40G>T	ENSP00000361400.2:p.Ala14Ser
ENST00000372327.9:c.40G>T	ENSP00000361402.5:p.Ala14Ser
ENST00000417041.1:c.40G>T	ENSP00000397375.1:p.Ala14Ser
ENST00000492049.1:c.40G>T	ENSP00000473275.1:p.Ala14Ser
NM_001098668.2:c.40G>T	NP_001092138.1:p.Ala14Ser
XM_005270128.2:c.91G>T	XP_005270185.1:p.Ala31Ser
XM_005270131.3:c.40G>T	XP_005270188.1:p.Ala14Ser
XM_005270132.3:c.40G>T	XP_005270189.1:p.Ala14Ser
XM_011540124.1:c.40G>T	XP_011538426.1:p.Ala14Ser
XM_011540125.1:c.40G>T	XP_011538427.1:p.Ala14Ser
NM_001098668.3:c.40G>T	NP_001092138.1:p.Ala14Ser
NM_001320813.1:c.40G>T	NP_001307742.1:p.Ala14Ser
NM_001320814.1:c.70G>T	NP_001307743.1:p.Ala24Ser
XM_005270128.3:c.91G>T	XP_005270185.1:p.Ala31Ser
XM_017016608.1:c.40G>T	XP_016872097.1:p.Ala14Ser
NM_001098668.4:c.40G>T MANE Select	NP_001092138.1:p.Ala14Ser
NM_001320813.2:c.40G>T	NP_001307742.1:p.Ala14Ser