Canonical Allele Identifier: CA2684616988

Gene: CFTR

Linked Data

• gnomAD v4: 7-117479985-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117479985A>G , CM000669.2:g.117479985A>G	GRCh38
NC_000007.13:g.117120039A>G , CM000669.1:g.117120039A>G	GRCh37
NC_000007.12:g.116907275A>G	NCBI36
NG_016465.4:g.19202A>G , LRG_663:g.19202A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446805.2:c.-191+291A>G	ENSP00000417012.1:n.-191+291A>G
ENST00000673785.1:c.-406+14154A>G	ENSP00000501235.1:n.-406+14154A>G
ENST00000003084.10:c.-110A>G	ENSP00000003084.6:n.-110A>G
ENST00000446805.1:c.-191+291A>G	ENSP00000417012.1:n.-191+291A>G
ENST00000546407.1:n.166+4177A>G
NM_000492.3:c.-110A>G , LRG_663t1:c.-110A>G	NP_000483.3:n.-110A>G
XM_011515751.1:c.143+640A>G	XP_011514053.1:n.143+640A>G
XM_011515752.1:c.143+640A>G	XP_011514054.1:n.143+640A>G
XM_011515753.1:c.-191+291A>G	XP_011514055.1:n.-191+291A>G
XM_011515754.1:c.-518-163A>G	XP_011514056.1:n.-518-163A>G