Canonical Allele Identifier: CA2574596517

Gene: SFTPA2

Linked Data

• gnomAD v4: 10-79557167-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79557167A>G , CM000672.2:g.79557167A>G	GRCh38
NC_000010.10:g.81316923A>G , CM000672.1:g.81316923A>G	GRCh37
NG_013046.1:g.8241T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000372325.7:c.*42T>C MANE Select	ENSP00000361400.2:n.*42T>C
ENST00000372325.6:c.*42T>C	ENSP00000361400.2:n.*42T>C
NM_001098668.2:c.*42T>C	NP_001092138.1:n.*42T>C
XM_005270128.2:c.*42T>C	XP_005270185.1:n.*42T>C
XM_005270131.3:c.*42T>C	XP_005270188.1:n.*42T>C
XM_005270132.3:c.*42T>C	XP_005270189.1:n.*42T>C
XM_011540124.1:c.*42T>C	XP_011538426.1:n.*42T>C
XM_011540125.1:c.*42T>C	XP_011538427.1:n.*42T>C
NM_001098668.3:c.*42T>C	NP_001092138.1:n.*42T>C
NM_001320813.1:c.*42T>C	NP_001307742.1:n.*42T>C
NM_001320814.1:c.*42T>C	NP_001307743.1:n.*42T>C
XM_005270128.3:c.*42T>C	XP_005270185.1:n.*42T>C
XM_017016608.1:c.*42T>C	XP_016872097.1:n.*42T>C
NM_001098668.4:c.*42T>C MANE Select	NP_001092138.1:n.*42T>C
NM_001320813.2:c.*42T>C	NP_001307742.1:n.*42T>C