Canonical Allele Identifier: CA1737344038
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479592G= , CM000669.2:g.117479592G= GRCh38
NC_000007.13:g.117119646G= , CM000669.1:g.117119646G= GRCh37
NC_000007.12:g.116906882G= NCBI36
NG_016465.4:g.18809G= , LRG_663:g.18809G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-293G= ENSP00000417012.1:n.-293G=
ENST00000673785.1:c.-406+13761G= ENSP00000501235.1:n.-406+13761G=
ENST00000446805.1:c.-293G= ENSP00000417012.1:n.-293G=
ENST00000546407.1:n.166+3784G=
XM_011515751.1:c.143+247G= XP_011514053.1:n.143+247G=
XM_011515752.1:c.143+247G= XP_011514054.1:n.143+247G=
XM_011515753.1:c.-293G= XP_011514055.1:n.-293G=
XM_011515754.1:c.-621G= XP_011514056.1:n.-621G=