Canonical Allele Identifier: CA470414439

Gene: SFTPA2

Linked Data

• MyVariant Identifiers: chr10:g.81316977G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79557221G>A , CM000672.2:g.79557221G>A	GRCh38
NC_000010.10:g.81316977G>A , CM000672.1:g.81316977G>A	GRCh37
NG_013046.1:g.8187C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372325.7:c.735C>T MANE Select	ENSP00000361400.2:p.Ile245=
ENST00000372325.6:c.735C>T	ENSP00000361400.2:p.Ile245=
ENST00000372327.9:c.735C>T	ENSP00000361402.5:p.Ile245=
NM_001098668.2:c.735C>T	NP_001092138.1:p.Ile245=
XM_005270128.2:c.786C>T	XP_005270185.1:p.Ile262=
XM_005270131.3:c.735C>T	XP_005270188.1:p.Ile245=
XM_005270132.3:c.735C>T	XP_005270189.1:p.Ile245=
XM_011540124.1:c.735C>T	XP_011538426.1:p.Ile245=
XM_011540125.1:c.735C>T	XP_011538427.1:p.Ile245=
NM_001098668.3:c.735C>T	NP_001092138.1:p.Ile245=
NM_001320813.1:c.735C>T	NP_001307742.1:p.Ile245=
NM_001320814.1:c.765C>T	NP_001307743.1:p.Ile255=
XM_005270128.3:c.786C>T	XP_005270185.1:p.Ile262=
XM_017016608.1:c.735C>T	XP_016872097.1:p.Ile245=
NM_001098668.4:c.735C>T MANE Select	NP_001092138.1:p.Ile245=
NM_001320813.2:c.735C>T	NP_001307742.1:p.Ile245=