Canonical Allele Identifier: CA1737344478

Gene: CFTR

Linked Data

• dbSNP Id: rs1797973785

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117480004del , CM000669.2:g.117480004del	GRCh38
NC_000007.13:g.117120058del , CM000669.1:g.117120058del	GRCh37
NC_000007.12:g.116907294del	NCBI36
NG_016465.4:g.19221del , LRG_663:g.19221del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.-91del	ENSP00000497673.2:n.-91del
ENST00000685018.2:c.-91del	ENSP00000510194.2:n.-91del
ENST00000687278.2:c.-91del	ENSP00000509593.2:n.-91del
ENST00000699585.1:c.-91del	ENSP00000514456.1:n.-91del
ENST00000699596.1:c.-91del	ENSP00000514465.1:n.-91del
ENST00000699597.1:c.-91del	ENSP00000514466.1:n.-91del
ENST00000699598.1:c.-91del	ENSP00000514467.1:n.-91del
ENST00000699599.1:c.-91del	ENSP00000514468.1:n.-91del
ENST00000699600.1:c.-91del	ENSP00000514469.1:n.-91del
ENST00000699601.1:c.-91del	ENSP00000514470.1:n.-91del
ENST00000699602.1:c.-91del	ENSP00000514471.1:n.-91del
ENST00000446805.2:c.-191+310del	ENSP00000417012.1:n.-191+310del
ENST00000673785.1:c.-406+14173del	ENSP00000501235.1:n.-406+14173del
ENST00000003084.10:c.-91del	ENSP00000003084.6:n.-91del
ENST00000446805.1:c.-191+310del	ENSP00000417012.1:n.-191+310del
ENST00000546407.1:n.166+4196del
NM_000492.3:c.-91del , LRG_663t1:c.-91del	NP_000483.3:n.-91del
XM_011515751.1:c.143+659del	XP_011514053.1:n.143+659del
XM_011515752.1:c.143+659del	XP_011514054.1:n.143+659del
XM_011515753.1:c.-191+310del	XP_011514055.1:n.-191+310del
XM_011515754.1:c.-518-144del	XP_011514056.1:n.-518-144del