Canonical Allele Identifier: CA2684617018
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117480024_117480025del , CM000669.2:g.117480024_117480025del GRCh38
NC_000007.13:g.117120078_117120079del , CM000669.1:g.117120078_117120079del GRCh37
NC_000007.12:g.116907314_116907315del NCBI36
NG_016465.4:g.19241_19242del , LRG_663:g.19241_19242del

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.-71_-70del ENSP00000497673.2:n.-71_-70del
ENST00000647978.2:c.-71_-70del ENSP00000497658.1:n.-71_-70del
ENST00000649781.2:c.-71_-70del ENSP00000497203.1:n.-71_-70del
ENST00000649850.2:c.-71_-70del ENSP00000514457.1:n.-71_-70del
ENST00000685018.2:c.-71_-70del ENSP00000510194.2:n.-71_-70del
ENST00000687278.2:c.-71_-70del ENSP00000509593.2:n.-71_-70del
ENST00000692802.2:n.14_15del
ENST00000693465.2:n.15_16del
ENST00000693480.2:n.14_15del
ENST00000699585.1:c.-71_-70del ENSP00000514456.1:n.-71_-70del
ENST00000699596.1:c.-71_-70del ENSP00000514465.1:n.-71_-70del
ENST00000699597.1:c.-71_-70del ENSP00000514466.1:n.-71_-70del
ENST00000699598.1:c.-71_-70del ENSP00000514467.1:n.-71_-70del
ENST00000699599.1:c.-71_-70del ENSP00000514468.1:n.-71_-70del
ENST00000699600.1:c.-71_-70del ENSP00000514469.1:n.-71_-70del
ENST00000699601.1:c.-71_-70del ENSP00000514470.1:n.-71_-70del
ENST00000699602.1:c.-71_-70del ENSP00000514471.1:n.-71_-70del
ENST00000699603.1:n.14_15del
ENST00000699604.1:c.-71_-70del ENSP00000514472.1:n.-71_-70del
ENST00000446805.2:c.-191+330_-191+331del ENSP00000417012.1:n.-191+330_-191+331del
ENST00000647639.1:n.14_15del
ENST00000647978.1:c.-71_-70del ENSP00000497658.1:n.-71_-70del
ENST00000648260.1:c.-71_-70del ENSP00000497957.1:n.-71_-70del
ENST00000649406.1:c.-71_-70del ENSP00000497965.1:n.-71_-70del
ENST00000649850.1:n.13_14del
ENST00000673785.1:c.-406+14193_-406+14194del ENSP00000501235.1:n.-406+14193_-406+14194del
ENST00000003084.10:c.-71_-70del ENSP00000003084.6:n.-71_-70del
ENST00000446805.1:c.-191+330_-191+331del ENSP00000417012.1:n.-191+330_-191+331del
ENST00000546407.1:n.166+4216_166+4217del
NM_000492.3:c.-71_-70del , LRG_663t1:c.-71_-70del NP_000483.3:n.-71_-70del
XM_011515751.1:c.143+679_143+680del XP_011514053.1:n.143+679_143+680del
XM_011515752.1:c.143+679_143+680del XP_011514054.1:n.143+679_143+680del
XM_011515753.1:c.-191+330_-191+331del XP_011514055.1:n.-191+330_-191+331del
XM_011515754.1:c.-518-124_-518-123del XP_011514056.1:n.-518-124_-518-123del