Canonical Allele Identifier: CA2684619754
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117504409_117504411del , CM000669.2:g.117504409_117504411del GRCh38
NC_000007.13:g.117144463_117144465del , CM000669.1:g.117144463_117144465del GRCh37
NC_000007.12:g.116931699_116931701del NCBI36
NG_016465.4:g.43626_43628del , LRG_663:g.43626_43628del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.164+46_164+48del ENSP00000497673.2:n.164+46_164+48del
ENST00000647978.2:c.164+46_164+48del ENSP00000497658.1:n.164+46_164+48del
ENST00000649781.2:c.164+46_164+48del ENSP00000497203.1:n.164+46_164+48del
ENST00000649850.2:c.164+46_164+48del ENSP00000514457.1:n.164+46_164+48del
ENST00000685018.2:c.164+46_164+48del ENSP00000510194.2:n.164+46_164+48del
ENST00000687278.2:c.164+46_164+48del ENSP00000509593.2:n.164+46_164+48del
ENST00000693465.2:n.249+46_249+48del
ENST00000699585.1:c.164+46_164+48del ENSP00000514456.1:n.164+46_164+48del
ENST00000699596.1:c.164+46_164+48del ENSP00000514465.1:n.164+46_164+48del
ENST00000699597.1:c.164+46_164+48del ENSP00000514466.1:n.164+46_164+48del
ENST00000699598.1:c.164+46_164+48del ENSP00000514467.1:n.164+46_164+48del
ENST00000699599.1:c.164+46_164+48del ENSP00000514468.1:n.164+46_164+48del
ENST00000699600.1:c.164+46_164+48del ENSP00000514469.1:n.164+46_164+48del
ENST00000699601.1:c.164+46_164+48del ENSP00000514470.1:n.164+46_164+48del
ENST00000699602.1:c.164+46_164+48del ENSP00000514471.1:n.164+46_164+48del
ENST00000699604.1:c.164+46_164+48del ENSP00000514472.1:n.164+46_164+48del
ENST00000699605.1:c.-80+46_-80+48del ENSP00000514473.1:n.-80+46_-80+48del
ENST00000446805.2:c.-80+46_-80+48del ENSP00000417012.1:n.-80+46_-80+48del
ENST00000693465.1:n.234+46_234+48del
ENST00000003084.11:c.164+46_164+48del MANE Select ENSP00000003084.6:n.164+46_164+48del
ENST00000647639.1:n.248+46_248+48del
ENST00000647978.1:c.164+46_164+48del ENSP00000497658.1:n.164+46_164+48del
ENST00000648260.1:c.164+46_164+48del ENSP00000497957.1:n.164+46_164+48del
ENST00000649406.1:c.164+46_164+48del ENSP00000497965.1:n.164+46_164+48del
ENST00000649781.1:c.164+46_164+48del ENSP00000497203.1:n.164+46_164+48del
ENST00000649850.1:n.247+46_247+48del
ENST00000673785.1:c.-80+46_-80+48del ENSP00000501235.1:n.-80+46_-80+48del
ENST00000003084.10:c.164+46_164+48del ENSP00000003084.6:n.164+46_164+48del
ENST00000426809.5:c.164+46_164+48del ENSP00000389119.1:n.164+46_164+48del
ENST00000446805.1:c.-80+46_-80+48del ENSP00000417012.1:n.-80+46_-80+48del
NM_000492.3:c.164+46_164+48del , LRG_663t1:c.164+46_164+48del NP_000483.3:n.164+46_164+48del
XM_011515751.1:c.254+46_254+48del XP_011514053.1:n.254+46_254+48del
XM_011515752.1:c.254+46_254+48del XP_011514054.1:n.254+46_254+48del
XM_011515753.1:c.-80+46_-80+48del XP_011514055.1:n.-80+46_-80+48del
XM_011515754.1:c.-154+46_-154+48del XP_011514056.1:n.-154+46_-154+48del
NM_000492.4:c.164+46_164+48del MANE Select NP_000483.3:n.164+46_164+48del