Canonical Allele Identifier: CA1737421502

Gene: CFTR

Linked Data

• dbSNP Id: rs1168652237

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117664536dup , CM000669.2:g.117664536dup	GRCh38
NC_000007.13:g.117304590dup , CM000669.1:g.117304590dup	GRCh37
NC_000007.12:g.117091826dup	NCBI36
NG_016465.4:g.203753dup , LRG_663:g.203753dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.*173-152dup	ENSP00000497673.2:n.*173-152dup
ENST00000647978.2:c.*3678-152dup	ENSP00000497658.1:n.*3678-152dup
ENST00000649781.2:c.3781-152dup	ENSP00000497203.1:n.3781-152dup
ENST00000685018.2:c.*177-152dup	ENSP00000510194.2:n.*177-152dup
ENST00000687278.2:c.*617-152dup	ENSP00000509593.2:n.*617-152dup
ENST00000699585.1:c.*173-152dup	ENSP00000514456.1:n.*173-152dup
ENST00000699598.1:c.3964-152dup	ENSP00000514467.1:n.3964-152dup
ENST00000699599.1:c.*177-152dup	ENSP00000514468.1:n.*177-152dup
ENST00000699600.1:c.*625-152dup	ENSP00000514469.1:n.*625-152dup
ENST00000699601.1:c.*2339-152dup	ENSP00000514470.1:n.*2339-152dup
ENST00000699602.1:c.3958-152dup	ENSP00000514471.1:n.3958-152dup
ENST00000699604.1:c.*3788-152dup	ENSP00000514472.1:n.*3788-152dup
ENST00000699605.1:c.3538-152dup	ENSP00000514473.1:n.3538-152dup
ENST00000699606.1:n.2132-152dup
ENST00000685018.1:c.828-152dup	ENSP00000510194.1:n.828-152dup
ENST00000687278.1:c.1751-152dup	ENSP00000509593.1:n.1751-152dup
ENST00000689011.1:c.546-152dup
ENST00000003084.11:c.3964-152dup MANE Select	ENSP00000003084.6:n.3964-152dup
ENST00000647720.1:c.1414-152dup
ENST00000649781.1:c.3781-152dup	ENSP00000497203.1:n.3781-152dup
ENST00000003084.10:c.3964-152dup	ENSP00000003084.6:n.3964-152dup
ENST00000426809.5:c.3874-152dup	ENSP00000389119.1:n.3874-152dup
ENST00000600166.1:c.90-152dup
NM_000492.3:c.3964-152dup , LRG_663t1:c.3964-152dup	NP_000483.3:n.3964-152dup
XM_011515751.1:c.4054-152dup	XP_011514053.1:n.4054-152dup
XM_011515752.1:c.4054-152dup	XP_011514054.1:n.4054-152dup
XM_011515753.1:c.3721-152dup	XP_011514055.1:n.3721-152dup
XM_011515754.1:c.3721-152dup	XP_011514056.1:n.3721-152dup
NM_000492.4:c.3964-152dup MANE Select	NP_000483.3:n.3964-152dup