Canonical Allele Identifier: CA1737343342
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478715T= , CM000669.2:g.117478715T= GRCh38
NC_000007.13:g.117118769T= , CM000669.1:g.117118769T= GRCh37
NC_000007.12:g.116906005T= NCBI36
NG_016465.4:g.17932T= , LRG_663:g.17932T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-526+293T= ENSP00000417012.1:n.-526+293T=
ENST00000673785.1:c.-406+12884T= ENSP00000501235.1:n.-406+12884T=
ENST00000546407.1:n.166+2907T=
XM_011515751.1:c.41+293T= XP_011514053.1:n.41+293T=
XM_011515752.1:c.41+293T= XP_011514054.1:n.41+293T=
XM_011515754.1:c.-1382T= XP_011514056.1:n.-1382T=