Canonical Allele Identifier: CA1770260215

Gene: SFTPC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22163902C= , CM000670.2:g.22163902C=	GRCh38
NC_000008.10:g.22021415C= , CM000670.1:g.22021415C=	GRCh37
NC_000008.9:g.22077360C=	NCBI36
NG_016968.1:g.7232C=
NG_029659.1:g.3763C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000679463.1:c.437C= MANE Select	ENSP00000505152.1:p.Ala146=
ENST00000318561.7:c.455C=	ENSP00000316152.3:p.Ala152=
ENST00000437090.6:c.*82C=	ENSP00000407931.2:n.*82C=
ENST00000520605.5:c.276+356C=	ENSP00000430266.1:n.276+356C=
ENST00000521315.5:c.437C=	ENSP00000430410.1:p.Ala146=
ENST00000522109.5:c.*338C=	ENSP00000429496.1:n.*338C=
ENST00000523296.1:c.278C=	ENSP00000429619.1:p.Ala93=
ENST00000524255.5:c.296C=	ENSP00000429552.1:p.Ala99=
NM_001172357.1:c.437C=	NP_001165828.1:p.Ala146=
NM_001172410.1:c.455C=	NP_001165881.1:p.Ala152=
NM_003018.3:c.455C=	NP_003009.2:p.Ala152=
XM_006716379.2:c.437C=	XP_006716442.1:p.Ala146=
XM_006716380.2:c.437C=	XP_006716443.1:p.Ala146=
XM_011544612.1:c.296C=	XP_011542914.1:p.Ala99=
XM_011544613.1:c.296C=	XP_011542915.1:p.Ala99=
NM_001317778.1:c.437C=	NP_001304707.1:p.Ala146=
NM_001317779.1:c.296C=	NP_001304708.1:p.Ala99=
NM_001317780.1:c.437C=	NP_001304709.1:p.Ala146=
XM_011544613.3:c.296C=	XP_011542915.1:p.Ala99=
NM_001172357.2:c.437C=	NP_001165828.1:p.Ala146=
NM_001172410.2:c.455C=	NP_001165881.1:p.Ala152=
NM_001317778.2:c.437C= MANE Select	NP_001304707.1:p.Ala146=
NM_001317779.2:c.296C=	NP_001304708.1:p.Ala99=
NM_001317780.2:c.437C=	NP_001304709.1:p.Ala146=
NM_003018.4:c.455C=	NP_003009.2:p.Ala152=
NM_001385653.1:c.455C=	NP_001372582.1:p.Ala152=
NM_001385654.1:c.455C=	NP_001372583.1:p.Ala152=
NM_001385655.1:c.455C=	NP_001372584.1:p.Ala152=
NM_001385656.1:c.437C=	NP_001372585.1:p.Ala146=
NM_001385657.1:c.437C=	NP_001372586.1:p.Ala146=
NM_001385658.1:c.437C=	NP_001372587.1:p.Ala146=
NM_001385659.1:c.437C=	NP_001372588.1:p.Ala146=
NM_001385660.1:c.296C=	NP_001372589.1:p.Ala99=