Canonical Allele Identifier: CA1737343561
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478943G= , CM000669.2:g.117478943G= GRCh38
NC_000007.13:g.117118997G= , CM000669.1:g.117118997G= GRCh37
NC_000007.12:g.116906233G= NCBI36
NG_016465.4:g.18160G= , LRG_663:g.18160G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-525-301G= ENSP00000417012.1:n.-525-301G=
ENST00000673785.1:c.-406+13112G= ENSP00000501235.1:n.-406+13112G=
ENST00000546407.1:n.166+3135G=
XM_011515751.1:c.42-301G= XP_011514053.1:n.42-301G=
XM_011515752.1:c.42-301G= XP_011514054.1:n.42-301G=
XM_011515754.1:c.-1154G= XP_011514056.1:n.-1154G=