Canonical Allele Identifier: CA210248434

Gene: SFTPA2

Linked Data

• dbSNP Id: rs952695410
• gnomAD v2: 10-81317317-A-G
• gnomAD v3: 10-79557561-A-G
• gnomAD v4: 10-79557561-A-G
• MyVariant Identifiers: chr10:g.81317317A>G (hg19) ; chr10:g.79557561A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79557561A>G , CM000672.2:g.79557561A>G	GRCh38
NC_000010.10:g.81317317A>G , CM000672.1:g.81317317A>G	GRCh37
NG_013046.1:g.7847T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372325.7:c.395T>C MANE Select	ENSP00000361400.2:p.Met132Thr
ENST00000372325.6:c.395T>C	ENSP00000361400.2:p.Met132Thr
ENST00000372327.9:c.395T>C	ENSP00000361402.5:p.Met132Thr
ENST00000417041.1:c.395T>C	ENSP00000397375.1:p.Met132Thr
NM_001098668.2:c.395T>C	NP_001092138.1:p.Met132Thr
XM_005270128.2:c.446T>C	XP_005270185.1:p.Met149Thr
XM_005270131.3:c.395T>C	XP_005270188.1:p.Met132Thr
XM_005270132.3:c.395T>C	XP_005270189.1:p.Met132Thr
XM_011540124.1:c.395T>C	XP_011538426.1:p.Met132Thr
XM_011540125.1:c.395T>C	XP_011538427.1:p.Met132Thr
NM_001098668.3:c.395T>C	NP_001092138.1:p.Met132Thr
NM_001320813.1:c.395T>C	NP_001307742.1:p.Met132Thr
NM_001320814.1:c.425T>C	NP_001307743.1:p.Met142Thr
XM_005270128.3:c.446T>C	XP_005270185.1:p.Met149Thr
XM_017016608.1:c.395T>C	XP_016872097.1:p.Met132Thr
NM_001098668.4:c.395T>C MANE Select	NP_001092138.1:p.Met132Thr
NM_001320813.2:c.395T>C	NP_001307742.1:p.Met132Thr