Canonical Allele Identifier: CA1737343712
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479200A= , CM000669.2:g.117479200A= GRCh38
NC_000007.13:g.117119254A= , CM000669.1:g.117119254A= GRCh37
NC_000007.12:g.116906490A= NCBI36
NG_016465.4:g.18417A= , LRG_663:g.18417A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-525-44A= ENSP00000417012.1:n.-525-44A=
ENST00000673785.1:c.-406+13369A= ENSP00000501235.1:n.-406+13369A=
ENST00000546407.1:n.166+3392A=
XM_011515751.1:c.42-44A= XP_011514053.1:n.42-44A=
XM_011515752.1:c.42-44A= XP_011514054.1:n.42-44A=
XM_011515754.1:c.-897A= XP_011514056.1:n.-897A=