Canonical Allele Identifier: CA368990606
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117610577T>A , CM000669.2:g.117610577T>A GRCh38
NC_000007.13:g.117250631T>A , CM000669.1:g.117250631T>A GRCh37
NC_000007.12:g.117037867T>A NCBI36
NG_016465.4:g.149794T>A , LRG_663:g.149794T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.3047T>A ENSP00000497673.2:p.Phe1016Tyr
ENST00000647978.2:c.*2761T>A ENSP00000497658.1:n.*2761T>A
ENST00000649781.2:c.2864T>A ENSP00000497203.1:p.Phe955Tyr
ENST00000685018.2:c.3047T>A ENSP00000510194.2:p.Phe1016Tyr
ENST00000687278.2:c.3047T>A ENSP00000509593.2:p.Phe1016Tyr
ENST00000699585.1:c.3047T>A ENSP00000514456.1:p.Phe1016Tyr
ENST00000699598.1:c.3047T>A ENSP00000514467.1:p.Phe1016Tyr
ENST00000699599.1:c.3047T>A ENSP00000514468.1:p.Phe1016Tyr
ENST00000699600.1:c.3047T>A ENSP00000514469.1:p.Phe1016Tyr
ENST00000699601.1:c.*1347T>A ENSP00000514470.1:n.*1347T>A
ENST00000699602.1:c.3047T>A ENSP00000514471.1:p.Phe1016Tyr
ENST00000699604.1:c.*2871T>A ENSP00000514472.1:n.*2871T>A
ENST00000699605.1:c.2621T>A ENSP00000514473.1:p.Phe874Tyr
ENST00000687278.1:c.638T>A ENSP00000509593.1:p.Phe213Tyr
ENST00000003084.11:c.3047T>A MANE Select ENSP00000003084.6:p.Phe1016Tyr
ENST00000647720.1:c.697T>A
ENST00000648260.1:c.1829T>A ENSP00000497957.1:p.Phe610Tyr
ENST00000649406.1:c.2864T>A ENSP00000497965.1:p.Phe955Tyr
ENST00000649781.1:c.2864T>A ENSP00000497203.1:p.Phe955Tyr
ENST00000003084.10:c.3047T>A ENSP00000003084.6:p.Phe1016Tyr
ENST00000426809.5:c.2957T>A ENSP00000389119.1:p.Phe986Tyr
NM_000492.3:c.3047T>A , LRG_663t1:c.3047T>A NP_000483.3:p.Phe1016Tyr
XM_011515751.1:c.3137T>A XP_011514053.1:p.Phe1046Tyr
XM_011515752.1:c.3137T>A XP_011514054.1:p.Phe1046Tyr
XM_011515753.1:c.2804T>A XP_011514055.1:p.Phe935Tyr
XM_011515754.1:c.2804T>A XP_011514056.1:p.Phe935Tyr
NM_000492.4:c.3047T>A MANE Select NP_000483.3:p.Phe1016Tyr