Canonical Allele Identifier: CA1266876940

Gene: SFTPB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85663483T= , CM000664.2:g.85663483T=	GRCh38
NC_000002.11:g.85890606T= , CM000664.1:g.85890606T=	GRCh37
NC_000002.10:g.85744117T=	NCBI36
NG_016967.1:g.10259A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409383.6:c.865A=	ENSP00000386346.2:p.Thr289=
ENST00000519937.7:c.865A= MANE Select	ENSP00000428719.2:p.Thr289=
ENST00000393822.7:c.865A=	ENSP00000377409.4:p.Thr289=
ENST00000409383.5:c.901A=	ENSP00000386346.1:p.Thr301=
ENST00000428225.5:c.846-4A=
ENST00000491167.1:n.65A=
ENST00000519937.6:c.865A=	ENSP00000428719.2:p.Thr289=
NM_000542.3:c.901A=	NP_000533.3:p.Thr301=
NM_198843.2:c.901A=	NP_942140.2:p.Thr301=
XM_005264487.2:c.901A=	XP_005264544.1:p.Thr301=
XM_005264488.2:c.857-4A=	XP_005264545.2:n.857-4A=
XM_005264490.3:c.865A=	XP_005264547.2:p.Thr289=
XM_005264488.4:c.857-4A=	XP_005264545.2:n.857-4A=
XM_005264490.4:c.865A=	XP_005264547.2:p.Thr289=
NM_000542.4:c.865A=	NP_000533.4:p.Thr289=
NM_001367281.1:c.865A=	NP_001354210.1:p.Thr289=
NM_198843.3:c.865A=	NP_942140.3:p.Thr289=
NM_000542.5:c.865A= MANE Select	NP_000533.4:p.Thr289=