Canonical Allele Identifier: CA1737344379
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479922A= , CM000669.2:g.117479922A= GRCh38
NC_000007.13:g.117119976A= , CM000669.1:g.117119976A= GRCh37
NC_000007.12:g.116907212A= NCBI36
NG_016465.4:g.19139A= , LRG_663:g.19139A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-191+228A= ENSP00000417012.1:n.-191+228A=
ENST00000673785.1:c.-406+14091A= ENSP00000501235.1:n.-406+14091A=
ENST00000446805.1:c.-191+228A= ENSP00000417012.1:n.-191+228A=
ENST00000546407.1:n.166+4114A=
XM_011515751.1:c.143+577A= XP_011514053.1:n.143+577A=
XM_011515752.1:c.143+577A= XP_011514054.1:n.143+577A=
XM_011515753.1:c.-191+228A= XP_011514055.1:n.-191+228A=
XM_011515754.1:c.-518-226A= XP_011514056.1:n.-518-226A=