Canonical Allele Identifier: CA1266878759

Gene: SFTPB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85666618G= , CM000664.2:g.85666618G=	GRCh38
NC_000002.11:g.85893741G= , CM000664.1:g.85893741G=	GRCh37
NC_000002.10:g.85747252G=	NCBI36
NG_016967.1:g.7124C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409383.6:c.392C=	ENSP00000386346.2:p.Thr131=
ENST00000519937.7:c.392C= MANE Select	ENSP00000428719.2:p.Thr131=
ENST00000393822.7:c.392C=	ENSP00000377409.4:p.Thr131=
ENST00000409383.5:c.428C=	ENSP00000386346.1:p.Thr143=
ENST00000428225.5:c.381C=
ENST00000473692.1:n.398C=
ENST00000519937.6:c.392C=	ENSP00000428719.2:p.Thr131=
NM_000542.3:c.428C=	NP_000533.3:p.Thr143=
NM_198843.2:c.428C=	NP_942140.2:p.Thr143=
XM_005264487.2:c.428C=	XP_005264544.1:p.Thr143=
XM_005264488.2:c.392C=	XP_005264545.2:p.Thr131=
XM_005264490.3:c.392C=	XP_005264547.2:p.Thr131=
XM_005264488.4:c.392C=	XP_005264545.2:p.Thr131=
XM_005264490.4:c.392C=	XP_005264547.2:p.Thr131=
NM_000542.4:c.392C=	NP_000533.4:p.Thr131=
NM_001367281.1:c.392C=	NP_001354210.1:p.Thr131=
NM_198843.3:c.392C=	NP_942140.3:p.Thr131=
NM_000542.5:c.392C= MANE Select	NP_000533.4:p.Thr131=