Canonical Allele Identifier: CA1737343434
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478827G= , CM000669.2:g.117478827G= GRCh38
NC_000007.13:g.117118881G= , CM000669.1:g.117118881G= GRCh37
NC_000007.12:g.116906117G= NCBI36
NG_016465.4:g.18044G= , LRG_663:g.18044G=

Transcript Alleles

HGVS Amino-acid change
ENST00000446805.2:c.-526+405G= ENSP00000417012.1:n.-526+405G=
ENST00000673785.1:c.-406+12996G= ENSP00000501235.1:n.-406+12996G=
ENST00000546407.1:n.166+3019G=
XM_011515751.1:c.41+405G= XP_011514053.1:n.41+405G=
XM_011515752.1:c.41+405G= XP_011514054.1:n.41+405G=
XM_011515754.1:c.-1270G= XP_011514056.1:n.-1270G=