Canonical Allele Identifier: CA1737343565
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478948T= , CM000669.2:g.117478948T= GRCh38
NC_000007.13:g.117119002T= , CM000669.1:g.117119002T= GRCh37
NC_000007.12:g.116906238T= NCBI36
NG_016465.4:g.18165T= , LRG_663:g.18165T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-525-296T= ENSP00000417012.1:n.-525-296T=
ENST00000673785.1:c.-406+13117T= ENSP00000501235.1:n.-406+13117T=
ENST00000546407.1:n.166+3140T=
XM_011515751.1:c.42-296T= XP_011514053.1:n.42-296T=
XM_011515752.1:c.42-296T= XP_011514054.1:n.42-296T=
XM_011515754.1:c.-1149T= XP_011514056.1:n.-1149T=