Canonical Allele Identifier: CA1737334634
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117541897_117541898delinsCT , CM000669.2:g.117541897_117541898delinsCT GRCh38
NC_000007.13:g.117181951_117181952delinsCT , CM000669.1:g.117181951_117181952delinsCT GRCh37
NC_000007.12:g.116969187_116969188delinsCT NCBI36
NG_016465.4:g.81114_81115delinsCT , LRG_663:g.81114_81115delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.1117-119_1117-118delinsCT ENSP00000497673.2:n.1117-119_1117-118deli...
ENST00000647978.2:c.*1014-119_*1014-118delinsCT ENSP00000497658.1:n.*1014-119_*1014-118de...
ENST00000649781.2:c.1117-119_1117-118delinsCT ENSP00000497203.1:n.1117-119_1117-118deli...
ENST00000685018.2:c.1117-119_1117-118delinsCT ENSP00000510194.2:n.1117-119_1117-118deli...
ENST00000687278.2:c.1117-119_1117-118delinsCT ENSP00000509593.2:n.1117-119_1117-118deli...
ENST00000699585.1:c.1117-119_1117-118delinsCT ENSP00000514456.1:n.1117-119_1117-118deli...
ENST00000699596.1:c.1117-119_1117-118delinsCT ENSP00000514465.1:n.1117-119_1117-118deli...
ENST00000699597.1:c.1117-119_1117-118delinsCT ENSP00000514466.1:n.1117-119_1117-118deli...
ENST00000699598.1:c.1117-119_1117-118delinsCT ENSP00000514467.1:n.1117-119_1117-118deli...
ENST00000699599.1:c.1117-119_1117-118delinsCT ENSP00000514468.1:n.1117-119_1117-118deli...
ENST00000699600.1:c.1117-119_1117-118delinsCT ENSP00000514469.1:n.1117-119_1117-118deli...
ENST00000699601.1:c.1117-119_1117-118delinsCT ENSP00000514470.1:n.1117-119_1117-118deli...
ENST00000699602.1:c.1117-119_1117-118delinsCT ENSP00000514471.1:n.1117-119_1117-118deli...
ENST00000699604.1:c.*941-119_*941-118delinsCT ENSP00000514472.1:n.*941-119_*941-118deli...
ENST00000699605.1:c.874-119_874-118delinsCT ENSP00000514473.1:n.874-119_874-118delins...
ENST00000003084.11:c.1117-119_1117-118delinsCT MANE Select ENSP00000003084.6:n.1117-119_1117-118deli...
ENST00000647978.1:c.*1014-119_*1014-118delinsCT ENSP00000497658.1:n.*1014-119_*1014-118de...
ENST00000648260.1:c.1117-119_1117-118delinsCT ENSP00000497957.1:n.1117-119_1117-118deli...
ENST00000649406.1:c.1117-119_1117-118delinsCT ENSP00000497965.1:n.1117-119_1117-118deli...
ENST00000649781.1:c.1117-119_1117-118delinsCT ENSP00000497203.1:n.1117-119_1117-118deli...
ENST00000673785.1:c.874-119_874-118delinsCT ENSP00000501235.1:n.874-119_874-118delins...
ENST00000003084.10:c.1117-119_1117-118delinsCT ENSP00000003084.6:n.1117-119_1117-118deli...
ENST00000426809.5:c.1027-119_1027-118delinsCT ENSP00000389119.1:n.1027-119_1027-118deli...
NM_000492.3:c.1117-119_1117-118delinsCT , LRG_663t1:c.1117-119_1117-118delinsCT NP_000483.3:n.1117-119_1117-118delinsCT
XM_011515751.1:c.1207-119_1207-118delinsCT XP_011514053.1:n.1207-119_1207-118delinsC...
XM_011515752.1:c.1207-119_1207-118delinsCT XP_011514054.1:n.1207-119_1207-118delinsC...
XM_011515753.1:c.874-119_874-118delinsCT XP_011514055.1:n.874-119_874-118delinsCT
XM_011515754.1:c.874-119_874-118delinsCT XP_011514056.1:n.874-119_874-118delinsCT
NM_000492.4:c.1117-119_1117-118delinsCT MANE Select NP_000483.3:n.1117-119_1117-118delinsCT