Canonical Allele Identifier: CA1737343908
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479445C= , CM000669.2:g.117479445C= GRCh38
NC_000007.13:g.117119499C= , CM000669.1:g.117119499C= GRCh37
NC_000007.12:g.116906735C= NCBI36
NG_016465.4:g.18662C= , LRG_663:g.18662C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-423-17C= ENSP00000417012.1:n.-423-17C=
ENST00000673785.1:c.-406+13614C= ENSP00000501235.1:n.-406+13614C=
ENST00000446805.1:c.-423-17C= ENSP00000417012.1:n.-423-17C=
ENST00000546407.1:n.166+3637C=
XM_011515751.1:c.143+100C= XP_011514053.1:n.143+100C=
XM_011515752.1:c.143+100C= XP_011514054.1:n.143+100C=
XM_011515753.1:c.-423-17C= XP_011514055.1:n.-423-17C=
XM_011515754.1:c.-751-17C= XP_011514056.1:n.-751-17C=