Canonical Allele Identifier: CA1737343592
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478980G= , CM000669.2:g.117478980G= GRCh38
NC_000007.13:g.117119034G= , CM000669.1:g.117119034G= GRCh37
NC_000007.12:g.116906270G= NCBI36
NG_016465.4:g.18197G= , LRG_663:g.18197G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-525-264G= ENSP00000417012.1:n.-525-264G=
ENST00000673785.1:c.-406+13149G= ENSP00000501235.1:n.-406+13149G=
ENST00000546407.1:n.166+3172G=
XM_011515751.1:c.42-264G= XP_011514053.1:n.42-264G=
XM_011515752.1:c.42-264G= XP_011514054.1:n.42-264G=
XM_011515754.1:c.-1117G= XP_011514056.1:n.-1117G=