Canonical Allele Identifier: CA1737343360
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478740T= , CM000669.2:g.117478740T= GRCh38
NC_000007.13:g.117118794T= , CM000669.1:g.117118794T= GRCh37
NC_000007.12:g.116906030T= NCBI36
NG_016465.4:g.17957T= , LRG_663:g.17957T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-526+318T= ENSP00000417012.1:n.-526+318T=
ENST00000673785.1:c.-406+12909T= ENSP00000501235.1:n.-406+12909T=
ENST00000546407.1:n.166+2932T=
XM_011515751.1:c.41+318T= XP_011514053.1:n.41+318T=
XM_011515752.1:c.41+318T= XP_011514054.1:n.41+318T=
XM_011515754.1:c.-1357T= XP_011514056.1:n.-1357T=