Canonical Allele Identifier: CA1737343376
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478750A= , CM000669.2:g.117478750A= GRCh38
NC_000007.13:g.117118804A= , CM000669.1:g.117118804A= GRCh37
NC_000007.12:g.116906040A= NCBI36
NG_016465.4:g.17967A= , LRG_663:g.17967A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-526+328A= ENSP00000417012.1:n.-526+328A=
ENST00000673785.1:c.-406+12919A= ENSP00000501235.1:n.-406+12919A=
ENST00000546407.1:n.166+2942A=
XM_011515751.1:c.41+328A= XP_011514053.1:n.41+328A=
XM_011515752.1:c.41+328A= XP_011514054.1:n.41+328A=
XM_011515754.1:c.-1347A= XP_011514056.1:n.-1347A=