Canonical Allele Identifier: CA368975502
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117642570A>G , CM000669.2:g.117642570A>G GRCh38
NC_000007.13:g.117282624A>G , CM000669.1:g.117282624A>G GRCh37
NC_000007.12:g.117069860A>G NCBI36
NG_016465.4:g.181787A>G , LRG_663:g.181787A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.*59A>G ENSP00000497673.2:n.*59A>G
ENST00000647978.2:c.*3564A>G ENSP00000497658.1:n.*3564A>G
ENST00000649781.2:c.3667A>G ENSP00000497203.1:p.Lys1223Glu
ENST00000685018.2:c.3850A>G ENSP00000510194.2:p.Lys1284Glu
ENST00000687278.2:c.*503A>G ENSP00000509593.2:n.*503A>G
ENST00000699585.1:c.*59A>G ENSP00000514456.1:n.*59A>G
ENST00000699598.1:c.3850A>G ENSP00000514467.1:p.Lys1284Glu
ENST00000699599.1:c.3850A>G ENSP00000514468.1:p.Lys1284Glu
ENST00000699600.1:c.*511A>G ENSP00000514469.1:n.*511A>G
ENST00000699601.1:c.*2225A>G ENSP00000514470.1:n.*2225A>G
ENST00000699602.1:c.3844A>G ENSP00000514471.1:p.Lys1282Glu
ENST00000699604.1:c.*3674A>G ENSP00000514472.1:n.*3674A>G
ENST00000699605.1:c.3424A>G ENSP00000514473.1:p.Lys1142Glu
ENST00000685018.1:c.598A>G ENSP00000510194.1:p.Lys200Glu
ENST00000687278.1:c.1637A>G ENSP00000509593.1:n.1637A>G
ENST00000689011.1:c.432A>G
ENST00000003084.11:c.3850A>G MANE Select ENSP00000003084.6:p.Lys1284Glu
ENST00000647720.1:c.1300A>G
ENST00000649781.1:c.3667A>G ENSP00000497203.1:p.Lys1223Glu
ENST00000003084.10:c.3850A>G ENSP00000003084.6:p.Lys1284Glu
ENST00000426809.5:c.3760A>G ENSP00000389119.1:p.Lys1254Glu
NM_000492.3:c.3850A>G , LRG_663t1:c.3850A>G NP_000483.3:p.Lys1284Glu
XM_011515751.1:c.3940A>G XP_011514053.1:p.Lys1314Glu
XM_011515752.1:c.3940A>G XP_011514054.1:p.Lys1314Glu
XM_011515753.1:c.3607A>G XP_011514055.1:p.Lys1203Glu
XM_011515754.1:c.3607A>G XP_011514056.1:p.Lys1203Glu
NM_000492.4:c.3850A>G MANE Select NP_000483.3:p.Lys1284Glu