Canonical Allele Identifier: CA1737343459
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478848G= , CM000669.2:g.117478848G= GRCh38
NC_000007.13:g.117118902G= , CM000669.1:g.117118902G= GRCh37
NC_000007.12:g.116906138G= NCBI36
NG_016465.4:g.18065G= , LRG_663:g.18065G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-525-396G= ENSP00000417012.1:n.-525-396G=
ENST00000673785.1:c.-406+13017G= ENSP00000501235.1:n.-406+13017G=
ENST00000546407.1:n.166+3040G=
XM_011515751.1:c.42-396G= XP_011514053.1:n.42-396G=
XM_011515752.1:c.42-396G= XP_011514054.1:n.42-396G=
XM_011515754.1:c.-1249G= XP_011514056.1:n.-1249G=