Canonical Allele Identifier: CA1744104

Gene: SFTPB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85666738G>A , CM000664.2:g.85666738G>A	GRCh38
NC_000002.11:g.85893861G>A , CM000664.1:g.85893861G>A	GRCh37
NC_000002.10:g.85747372G>A	NCBI36
NG_016967.1:g.7004C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000542.5:c.272C>T MANE Select	NP_000533.4:p.Thr91Met
ENST00000519937.7:c.272C>T MANE Select	ENSP00000428719.2:p.Thr91Met
NM_000542.3:c.308C>T	NP_000533.3:p.Thr103Met
NM_000542.4:c.272C>T	NP_000533.4:p.Thr91Met
NM_001367281.1:c.272C>T	NP_001354210.1:p.Thr91Met
NM_198843.2:c.308C>T	NP_942140.2:p.Thr103Met
NM_198843.3:c.272C>T	NP_942140.3:p.Thr91Met
ENST00000393822.7:c.272C>T	ENSP00000377409.4:p.Thr91Met
ENST00000409383.5:c.308C>T	ENSP00000386346.1:p.Thr103Met
ENST00000409383.6:c.272C>T	ENSP00000386346.2:p.Thr91Met
ENST00000428225.5:c.261C>T
ENST00000473692.1:n.278C>T
ENST00000519937.6:c.272C>T	ENSP00000428719.2:p.Thr91Met
XM_005264487.2:c.308C>T	XP_005264544.1:p.Thr103Met
XM_005264488.2:c.272C>T	XP_005264545.2:p.Thr91Met
XM_005264488.4:c.272C>T	XP_005264545.2:p.Thr91Met
XM_005264490.3:c.272C>T	XP_005264547.2:p.Thr91Met
XM_005264490.4:c.272C>T	XP_005264547.2:p.Thr91Met