Canonical Allele Identifier: CA368996316
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117627592A>G , CM000669.2:g.117627592A>G GRCh38
NC_000007.13:g.117267646A>G , CM000669.1:g.117267646A>G GRCh37
NC_000007.12:g.117054882A>G NCBI36
NG_016465.4:g.166809A>G , LRG_663:g.166809A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.3517+22A>G ENSP00000497673.2:n.3517+22A>G
ENST00000647978.2:c.*3253A>G ENSP00000497658.1:n.*3253A>G
ENST00000649781.2:c.3356A>G ENSP00000497203.1:p.Lys1119Arg
ENST00000685018.2:c.3539A>G ENSP00000510194.2:p.Lys1180Arg
ENST00000687278.2:c.*192A>G ENSP00000509593.2:n.*192A>G
ENST00000699585.1:c.3517+22A>G ENSP00000514456.1:n.3517+22A>G
ENST00000699598.1:c.3539A>G ENSP00000514467.1:p.Lys1180Arg
ENST00000699599.1:c.3539A>G ENSP00000514468.1:p.Lys1180Arg
ENST00000699600.1:c.*200A>G ENSP00000514469.1:n.*200A>G
ENST00000699601.1:c.*1914A>G ENSP00000514470.1:n.*1914A>G
ENST00000699602.1:c.3533A>G ENSP00000514471.1:p.Lys1178Arg
ENST00000699604.1:c.*3363A>G ENSP00000514472.1:n.*3363A>G
ENST00000699605.1:c.3113A>G ENSP00000514473.1:p.Lys1038Arg
ENST00000685018.1:c.287A>G ENSP00000510194.1:p.Lys96Arg
ENST00000687278.1:c.1326A>G ENSP00000509593.1:n.1326A>G
ENST00000689011.1:c.121A>G
ENST00000003084.11:c.3539A>G MANE Select ENSP00000003084.6:p.Lys1180Arg
ENST00000647720.1:c.1167+22A>G
ENST00000648260.1:c.2321A>G ENSP00000497957.1:p.Lys774Arg
ENST00000649406.1:c.3356A>G ENSP00000497965.1:p.Lys1119Arg
ENST00000649781.1:c.3356A>G ENSP00000497203.1:p.Lys1119Arg
ENST00000003084.10:c.3539A>G ENSP00000003084.6:p.Lys1180Arg
ENST00000426809.5:c.3449A>G ENSP00000389119.1:p.Lys1150Arg
ENST00000468795.1:c.364A>G
NM_000492.3:c.3539A>G , LRG_663t1:c.3539A>G NP_000483.3:p.Lys1180Arg
XM_011515751.1:c.3629A>G XP_011514053.1:p.Lys1210Arg
XM_011515752.1:c.3629A>G XP_011514054.1:p.Lys1210Arg
XM_011515753.1:c.3296A>G XP_011514055.1:p.Lys1099Arg
XM_011515754.1:c.3296A>G XP_011514056.1:p.Lys1099Arg
NM_000492.4:c.3539A>G MANE Select NP_000483.3:p.Lys1180Arg