Canonical Allele Identifier: CA460170839

Gene: SFTPC

Linked Data

• gnomAD v4: 8-22164032-C-T
• MyVariant Identifiers: chr8:g.22021545C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.22164032C>T , CM000670.2:g.22164032C>T	GRCh38
NC_000008.10:g.22021545C>T , CM000670.1:g.22021545C>T	GRCh37
NC_000008.9:g.22077490C>T	NCBI36
NG_016968.1:g.7362C>T
NG_029659.1:g.3893C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000679463.1:c.567C>T MANE Select	ENSP00000505152.1:p.Tyr189=
ENST00000318561.7:c.585C>T	ENSP00000316152.3:p.Tyr195=
ENST00000437090.6:c.*212C>T	ENSP00000407931.2:n.*212C>T
ENST00000520605.5:c.277-234C>T	ENSP00000430266.1:n.277-234C>T
ENST00000521315.5:c.567C>T	ENSP00000430410.1:p.Tyr189=
ENST00000524255.5:c.426C>T	ENSP00000429552.1:p.Tyr142=
NM_001172357.1:c.567C>T	NP_001165828.1:p.Tyr189=
NM_001172410.1:c.585C>T	NP_001165881.1:p.Tyr195=
NM_003018.3:c.585C>T	NP_003009.2:p.Tyr195=
XM_006716379.2:c.567C>T	XP_006716442.1:p.Tyr189=
XM_006716380.2:c.567C>T	XP_006716443.1:p.Tyr189=
XM_011544612.1:c.426C>T	XP_011542914.1:p.Tyr142=
XM_011544613.1:c.426C>T	XP_011542915.1:p.Tyr142=
NM_001317778.1:c.567C>T	NP_001304707.1:p.Tyr189=
NM_001317779.1:c.426C>T	NP_001304708.1:p.Tyr142=
NM_001317780.1:c.567C>T	NP_001304709.1:p.Tyr189=
XM_011544613.3:c.426C>T	XP_011542915.1:p.Tyr142=
NM_001172357.2:c.567C>T	NP_001165828.1:p.Tyr189=
NM_001172410.2:c.585C>T	NP_001165881.1:p.Tyr195=
NM_001317778.2:c.567C>T MANE Select	NP_001304707.1:p.Tyr189=
NM_001317779.2:c.426C>T	NP_001304708.1:p.Tyr142=
NM_001317780.2:c.567C>T	NP_001304709.1:p.Tyr189=
NM_003018.4:c.585C>T	NP_003009.2:p.Tyr195=
NM_001385653.1:c.585C>T	NP_001372582.1:p.Tyr195=
NM_001385654.1:c.585C>T	NP_001372583.1:p.Tyr195=
NM_001385655.1:c.585C>T	NP_001372584.1:p.Tyr195=
NM_001385656.1:c.567C>T	NP_001372585.1:p.Tyr189=
NM_001385657.1:c.567C>T	NP_001372586.1:p.Tyr189=
NM_001385658.1:c.567C>T	NP_001372587.1:p.Tyr189=
NM_001385659.1:c.567C>T	NP_001372588.1:p.Tyr189=
NM_001385660.1:c.426C>T	NP_001372589.1:p.Tyr142=