Canonical Allele Identifier: CA1922240752

Gene: SFTPA2

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.79557317T= , CM000672.2:g.79557317T=	GRCh38
NC_000010.10:g.81317073T= , CM000672.1:g.81317073T=	GRCh37
NG_013046.1:g.8091A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372325.7:c.639A= MANE Select	ENSP00000361400.2:p.Arg213=
ENST00000372325.6:c.639A=	ENSP00000361400.2:p.Arg213=
ENST00000372327.9:c.639A=	ENSP00000361402.5:p.Arg213=
NM_001098668.2:c.639A=	NP_001092138.1:p.Arg213=
XM_005270128.2:c.690A=	XP_005270185.1:p.Arg230=
XM_005270131.3:c.639A=	XP_005270188.1:p.Arg213=
XM_005270132.3:c.639A=	XP_005270189.1:p.Arg213=
XM_011540124.1:c.639A=	XP_011538426.1:p.Arg213=
XM_011540125.1:c.639A=	XP_011538427.1:p.Arg213=
NM_001098668.3:c.639A=	NP_001092138.1:p.Arg213=
NM_001320813.1:c.639A=	NP_001307742.1:p.Arg213=
NM_001320814.1:c.669A=	NP_001307743.1:p.Arg223=
XM_005270128.3:c.690A=	XP_005270185.1:p.Arg230=
XM_017016608.1:c.639A=	XP_016872097.1:p.Arg213=
NM_001098668.4:c.639A= MANE Select	NP_001092138.1:p.Arg213=
NM_001320813.2:c.639A=	NP_001307742.1:p.Arg213=