Canonical Allele Identifier: CA370538390
Gene: SFTPC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.22163985T>A , CM000670.2:g.22163985T>A GRCh38
NC_000008.10:g.22021498T>A , CM000670.1:g.22021498T>A GRCh37
NC_000008.9:g.22077443T>A NCBI36
NG_016968.1:g.7315T>A
NG_029659.1:g.3846T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000679463.1:c.520T>A MANE Select ENSP00000505152.1:p.Phe174Ile
ENST00000318561.7:c.538T>A ENSP00000316152.3:p.Phe180Ile
ENST00000437090.6:c.*165T>A ENSP00000407931.2:n.*165T>A
ENST00000520605.5:c.277-281T>A ENSP00000430266.1:n.277-281T>A
ENST00000521315.5:c.520T>A ENSP00000430410.1:p.Phe174Ile
ENST00000522109.5:c.*421T>A ENSP00000429496.1:n.*421T>A
ENST00000523296.1:c.361T>A ENSP00000429619.1:p.Phe121Ile
ENST00000524255.5:c.379T>A ENSP00000429552.1:p.Phe127Ile
NM_001172357.1:c.520T>A NP_001165828.1:p.Phe174Ile
NM_001172410.1:c.538T>A NP_001165881.1:p.Phe180Ile
NM_003018.3:c.538T>A NP_003009.2:p.Phe180Ile
XM_006716379.2:c.520T>A XP_006716442.1:p.Phe174Ile
XM_006716380.2:c.520T>A XP_006716443.1:p.Phe174Ile
XM_011544612.1:c.379T>A XP_011542914.1:p.Phe127Ile
XM_011544613.1:c.379T>A XP_011542915.1:p.Phe127Ile
NM_001317778.1:c.520T>A NP_001304707.1:p.Phe174Ile
NM_001317779.1:c.379T>A NP_001304708.1:p.Phe127Ile
NM_001317780.1:c.520T>A NP_001304709.1:p.Phe174Ile
XM_011544613.3:c.379T>A XP_011542915.1:p.Phe127Ile
NM_001172357.2:c.520T>A NP_001165828.1:p.Phe174Ile
NM_001172410.2:c.538T>A NP_001165881.1:p.Phe180Ile
NM_001317778.2:c.520T>A MANE Select NP_001304707.1:p.Phe174Ile
NM_001317779.2:c.379T>A NP_001304708.1:p.Phe127Ile
NM_001317780.2:c.520T>A NP_001304709.1:p.Phe174Ile
NM_003018.4:c.538T>A NP_003009.2:p.Phe180Ile
NM_001385653.1:c.538T>A NP_001372582.1:p.Phe180Ile
NM_001385654.1:c.538T>A NP_001372583.1:p.Phe180Ile
NM_001385655.1:c.538T>A NP_001372584.1:p.Phe180Ile
NM_001385656.1:c.520T>A NP_001372585.1:p.Phe174Ile
NM_001385657.1:c.520T>A NP_001372586.1:p.Phe174Ile
NM_001385658.1:c.520T>A NP_001372587.1:p.Phe174Ile
NM_001385659.1:c.520T>A NP_001372588.1:p.Phe174Ile
NM_001385660.1:c.379T>A NP_001372589.1:p.Phe127Ile