Canonical Allele Identifier: CA1737343911
Gene: CFTR HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479446C= , CM000669.2:g.117479446C= GRCh38
NC_000007.13:g.117119500C= , CM000669.1:g.117119500C= GRCh37
NC_000007.12:g.116906736C= NCBI36
NG_016465.4:g.18663C= , LRG_663:g.18663C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-423-16C= ENSP00000417012.1:n.-423-16C=
ENST00000673785.1:c.-406+13615C= ENSP00000501235.1:n.-406+13615C=
ENST00000446805.1:c.-423-16C= ENSP00000417012.1:n.-423-16C=
ENST00000546407.1:n.166+3638C=
XM_011515751.1:c.143+101C= XP_011514053.1:n.143+101C=
XM_011515752.1:c.143+101C= XP_011514054.1:n.143+101C=
XM_011515753.1:c.-423-16C= XP_011514055.1:n.-423-16C=
XM_011515754.1:c.-751-16C= XP_011514056.1:n.-751-16C=
Search 100 bp 5'
Search 100 bp 3'