Canonical Allele Identifier: CA1737343367
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478746G= , CM000669.2:g.117478746G= GRCh38
NC_000007.13:g.117118800G= , CM000669.1:g.117118800G= GRCh37
NC_000007.12:g.116906036G= NCBI36
NG_016465.4:g.17963G= , LRG_663:g.17963G=

Transcript Alleles

HGVS Amino-acid change
ENST00000446805.2:c.-526+324G= ENSP00000417012.1:n.-526+324G=
ENST00000673785.1:c.-406+12915G= ENSP00000501235.1:n.-406+12915G=
ENST00000546407.1:n.166+2938G=
XM_011515751.1:c.41+324G= XP_011514053.1:n.41+324G=
XM_011515752.1:c.41+324G= XP_011514054.1:n.41+324G=
XM_011515754.1:c.-1351G= XP_011514056.1:n.-1351G=