Canonical Allele Identifier: CA1737343786
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479302A= , CM000669.2:g.117479302A= GRCh38
NC_000007.13:g.117119356A= , CM000669.1:g.117119356A= GRCh37
NC_000007.12:g.116906592A= NCBI36
NG_016465.4:g.18519A= , LRG_663:g.18519A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-467A= ENSP00000417012.1:n.-467A=
ENST00000673785.1:c.-406+13471A= ENSP00000501235.1:n.-406+13471A=
ENST00000546407.1:n.166+3494A=
XM_011515751.1:c.100A= XP_011514053.1:p.Ile34=
XM_011515752.1:c.100A= XP_011514054.1:p.Ile34=
XM_011515754.1:c.-795A= XP_011514056.1:n.-795A=