Canonical Allele Identifier: CA1266876916

Gene: SFTPB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85663440A= , CM000664.2:g.85663440A=	GRCh38
NC_000002.11:g.85890563A= , CM000664.1:g.85890563A=	GRCh37
NC_000002.10:g.85744074A=	NCBI36
NG_016967.1:g.10302T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409383.6:c.908T=	ENSP00000386346.2:p.Met303=
ENST00000519937.7:c.908T= MANE Select	ENSP00000428719.2:p.Met303=
ENST00000393822.7:c.908T=	ENSP00000377409.4:p.Met303=
ENST00000409383.5:c.944T=	ENSP00000386346.1:p.Met315=
ENST00000428225.5:c.885T=
ENST00000491167.1:n.108T=
ENST00000494165.1:c.39T=
ENST00000519937.6:c.908T=	ENSP00000428719.2:p.Met303=
NM_000542.3:c.944T=	NP_000533.3:p.Met315=
NM_198843.2:c.944T=	NP_942140.2:p.Met315=
XM_005264487.2:c.944T=	XP_005264544.1:p.Met315=
XM_005264488.2:c.896T=	XP_005264545.2:p.Met299=
XM_005264490.3:c.908T=	XP_005264547.2:p.Met303=
XM_005264488.4:c.896T=	XP_005264545.2:p.Met299=
XM_005264490.4:c.908T=	XP_005264547.2:p.Met303=
NM_000542.4:c.908T=	NP_000533.4:p.Met303=
NM_001367281.1:c.908T=	NP_001354210.1:p.Met303=
NM_198843.3:c.908T=	NP_942140.3:p.Met303=
NM_000542.5:c.908T= MANE Select	NP_000533.4:p.Met303=