Canonical Allele Identifier: CA1737361668
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117534218_117534223delinsTTATAA , CM000669.2:g.117534218_117534223delinsTTATAA GRCh38
NC_000007.13:g.117174272_117174277delinsTTATAA , CM000669.1:g.117174272_117174277delinsTTATAA GRCh37
NC_000007.12:g.116961508_116961513delinsTTATAA NCBI36
NG_016465.4:g.73435_73440delinsTTATAA , LRG_663:g.73435_73440delinsTTATAA

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.490-58_490-53delinsTTATAA ENSP00000497673.2:n.490-58_490-53delinsTT...
ENST00000647978.2:c.*387-58_*387-53delinsTTATAA ENSP00000497658.1:n.*387-58_*387-53delins...
ENST00000649781.2:c.490-58_490-53delinsTTATAA ENSP00000497203.1:n.490-58_490-53delinsTT...
ENST00000685018.2:c.490-58_490-53delinsTTATAA ENSP00000510194.2:n.490-58_490-53delinsTT...
ENST00000687278.2:c.490-58_490-53delinsTTATAA ENSP00000509593.2:n.490-58_490-53delinsTT...
ENST00000699585.1:c.490-58_490-53delinsTTATAA ENSP00000514456.1:n.490-58_490-53delinsTT...
ENST00000699596.1:c.490-58_490-53delinsTTATAA ENSP00000514465.1:n.490-58_490-53delinsTT...
ENST00000699597.1:c.490-58_490-53delinsTTATAA ENSP00000514466.1:n.490-58_490-53delinsTT...
ENST00000699598.1:c.490-58_490-53delinsTTATAA ENSP00000514467.1:n.490-58_490-53delinsTT...
ENST00000699599.1:c.490-58_490-53delinsTTATAA ENSP00000514468.1:n.490-58_490-53delinsTT...
ENST00000699600.1:c.490-58_490-53delinsTTATAA ENSP00000514469.1:n.490-58_490-53delinsTT...
ENST00000699601.1:c.490-58_490-53delinsTTATAA ENSP00000514470.1:n.490-58_490-53delinsTT...
ENST00000699602.1:c.490-58_490-53delinsTTATAA ENSP00000514471.1:n.490-58_490-53delinsTT...
ENST00000699604.1:c.*314-58_*314-53delinsTTATAA ENSP00000514472.1:n.*314-58_*314-53delins...
ENST00000699605.1:c.247-58_247-53delinsTTATAA ENSP00000514473.1:n.247-58_247-53delinsTT...
ENST00000003084.11:c.490-58_490-53delinsTTATAA MANE Select ENSP00000003084.6:n.490-58_490-53delinsTT...
ENST00000647978.1:c.*387-58_*387-53delinsTTATAA ENSP00000497658.1:n.*387-58_*387-53delins...
ENST00000648260.1:c.490-58_490-53delinsTTATAA ENSP00000497957.1:n.490-58_490-53delinsTT...
ENST00000649406.1:c.490-58_490-53delinsTTATAA ENSP00000497965.1:n.490-58_490-53delinsTT...
ENST00000649781.1:c.490-58_490-53delinsTTATAA ENSP00000497203.1:n.490-58_490-53delinsTT...
ENST00000673785.1:c.247-58_247-53delinsTTATAA ENSP00000501235.1:n.247-58_247-53delinsTT...
ENST00000003084.10:c.490-58_490-53delinsTTATAA ENSP00000003084.6:n.490-58_490-53delinsTT...
ENST00000426809.5:c.490-1030_490-1025delinsTTATAA ENSP00000389119.1:n.490-1030_490-1025deli...
NM_000492.3:c.490-58_490-53delinsTTATAA , LRG_663t1:c.490-58_490-53delinsTTATAA NP_000483.3:n.490-58_490-53delinsTTATAA
XM_011515751.1:c.580-58_580-53delinsTTATAA XP_011514053.1:n.580-58_580-53delinsTTATA...
XM_011515752.1:c.580-58_580-53delinsTTATAA XP_011514054.1:n.580-58_580-53delinsTTATA...
XM_011515753.1:c.247-58_247-53delinsTTATAA XP_011514055.1:n.247-58_247-53delinsTTATA...
XM_011515754.1:c.247-58_247-53delinsTTATAA XP_011514056.1:n.247-58_247-53delinsTTATA...
NM_000492.4:c.490-58_490-53delinsTTATAA MANE Select NP_000483.3:n.490-58_490-53delinsTTATAA