Canonical Allele Identifier: CA1737334629
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117541894_117541897delinsTTAC , CM000669.2:g.117541894_117541897delinsTTAC GRCh38
NC_000007.13:g.117181948_117181951delinsTTAC , CM000669.1:g.117181948_117181951delinsTTAC GRCh37
NC_000007.12:g.116969184_116969187delinsTTAC NCBI36
NG_016465.4:g.81111_81114delinsTTAC , LRG_663:g.81111_81114delinsTTAC

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.1117-122_1117-119delinsTTAC ENSP00000497673.2:n.1117-122_1117-119deli...
ENST00000647978.2:c.*1014-122_*1014-119delinsTTAC ENSP00000497658.1:n.*1014-122_*1014-119de...
ENST00000649781.2:c.1117-122_1117-119delinsTTAC ENSP00000497203.1:n.1117-122_1117-119deli...
ENST00000685018.2:c.1117-122_1117-119delinsTTAC ENSP00000510194.2:n.1117-122_1117-119deli...
ENST00000687278.2:c.1117-122_1117-119delinsTTAC ENSP00000509593.2:n.1117-122_1117-119deli...
ENST00000699585.1:c.1117-122_1117-119delinsTTAC ENSP00000514456.1:n.1117-122_1117-119deli...
ENST00000699596.1:c.1117-122_1117-119delinsTTAC ENSP00000514465.1:n.1117-122_1117-119deli...
ENST00000699597.1:c.1117-122_1117-119delinsTTAC ENSP00000514466.1:n.1117-122_1117-119deli...
ENST00000699598.1:c.1117-122_1117-119delinsTTAC ENSP00000514467.1:n.1117-122_1117-119deli...
ENST00000699599.1:c.1117-122_1117-119delinsTTAC ENSP00000514468.1:n.1117-122_1117-119deli...
ENST00000699600.1:c.1117-122_1117-119delinsTTAC ENSP00000514469.1:n.1117-122_1117-119deli...
ENST00000699601.1:c.1117-122_1117-119delinsTTAC ENSP00000514470.1:n.1117-122_1117-119deli...
ENST00000699602.1:c.1117-122_1117-119delinsTTAC ENSP00000514471.1:n.1117-122_1117-119deli...
ENST00000699604.1:c.*941-122_*941-119delinsTTAC ENSP00000514472.1:n.*941-122_*941-119deli...
ENST00000699605.1:c.874-122_874-119delinsTTAC ENSP00000514473.1:n.874-122_874-119delins...
ENST00000003084.11:c.1117-122_1117-119delinsTTAC MANE Select ENSP00000003084.6:n.1117-122_1117-119deli...
ENST00000647978.1:c.*1014-122_*1014-119delinsTTAC ENSP00000497658.1:n.*1014-122_*1014-119de...
ENST00000648260.1:c.1117-122_1117-119delinsTTAC ENSP00000497957.1:n.1117-122_1117-119deli...
ENST00000649406.1:c.1117-122_1117-119delinsTTAC ENSP00000497965.1:n.1117-122_1117-119deli...
ENST00000649781.1:c.1117-122_1117-119delinsTTAC ENSP00000497203.1:n.1117-122_1117-119deli...
ENST00000673785.1:c.874-122_874-119delinsTTAC ENSP00000501235.1:n.874-122_874-119delins...
ENST00000003084.10:c.1117-122_1117-119delinsTTAC ENSP00000003084.6:n.1117-122_1117-119deli...
ENST00000426809.5:c.1027-122_1027-119delinsTTAC ENSP00000389119.1:n.1027-122_1027-119deli...
NM_000492.3:c.1117-122_1117-119delinsTTAC , LRG_663t1:c.1117-122_1117-119delinsTTAC NP_000483.3:n.1117-122_1117-119delinsTTAC...
XM_011515751.1:c.1207-122_1207-119delinsTTAC XP_011514053.1:n.1207-122_1207-119delinsT...
XM_011515752.1:c.1207-122_1207-119delinsTTAC XP_011514054.1:n.1207-122_1207-119delinsT...
XM_011515753.1:c.874-122_874-119delinsTTAC XP_011514055.1:n.874-122_874-119delinsTTA...
XM_011515754.1:c.874-122_874-119delinsTTAC XP_011514056.1:n.874-122_874-119delinsTTA...
NM_000492.4:c.1117-122_1117-119delinsTTAC MANE Select NP_000483.3:n.1117-122_1117-119delinsTTAC...