Canonical Allele Identifier: CA1266876953

Gene: SFTPB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85663509_85663510delinsAG , CM000664.2:g.85663509_85663510delinsAG	GRCh38
NC_000002.11:g.85890632_85890633delinsAG , CM000664.1:g.85890632_85890633delinsAG	GRCh37
NC_000002.10:g.85744143_85744144delinsAG	NCBI36
NG_016967.1:g.10232_10233delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409383.6:c.857-19_857-18delinsCT	ENSP00000386346.2:n.857-19_857-18delinsCT
ENST00000519937.7:c.857-19_857-18delinsCT MANE Select	ENSP00000428719.2:n.857-19_857-18delinsCT
ENST00000393822.7:c.857-19_857-18delinsCT	ENSP00000377409.4:n.857-19_857-18delinsCT
ENST00000409383.5:c.893-19_893-18delinsCT	ENSP00000386346.1:n.893-19_893-18delinsCT
ENST00000428225.5:c.846-31_846-30delinsCT
ENST00000491167.1:n.38_39delinsCT
ENST00000519937.6:c.857-19_857-18delinsCT	ENSP00000428719.2:n.857-19_857-18delinsCT
NM_000542.3:c.893-19_893-18delinsCT	NP_000533.3:n.893-19_893-18delinsCT
NM_198843.2:c.893-19_893-18delinsCT	NP_942140.2:n.893-19_893-18delinsCT
XM_005264487.2:c.893-19_893-18delinsCT	XP_005264544.1:n.893-19_893-18delinsCT
XM_005264488.2:c.857-31_857-30delinsCT	XP_005264545.2:n.857-31_857-30delinsCT
XM_005264490.3:c.857-19_857-18delinsCT	XP_005264547.2:n.857-19_857-18delinsCT
XM_005264488.4:c.857-31_857-30delinsCT	XP_005264545.2:n.857-31_857-30delinsCT
XM_005264490.4:c.857-19_857-18delinsCT	XP_005264547.2:n.857-19_857-18delinsCT
NM_000542.4:c.857-19_857-18delinsCT	NP_000533.4:n.857-19_857-18delinsCT
NM_001367281.1:c.857-19_857-18delinsCT	NP_001354210.1:n.857-19_857-18delinsCT
NM_198843.3:c.857-19_857-18delinsCT	NP_942140.3:n.857-19_857-18delinsCT
NM_000542.5:c.857-19_857-18delinsCT MANE Select	NP_000533.4:n.857-19_857-18delinsCT