Canonical Allele Identifier: CA1737421500

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117664532_117664533delinsCT , CM000669.2:g.117664532_117664533delinsCT	GRCh38
NC_000007.13:g.117304586_117304587delinsCT , CM000669.1:g.117304586_117304587delinsCT	GRCh37
NC_000007.12:g.117091822_117091823delinsCT	NCBI36
NG_016465.4:g.203749_203750delinsCT , LRG_663:g.203749_203750delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.*173-156_*173-155delinsCT	ENSP00000497673.2:n.*173-156_*173-155delinsCT
ENST00000647978.2:c.*3678-156_*3678-155delinsCT	ENSP00000497658.1:n.*3678-156_*3678-155delinsCT
ENST00000649781.2:c.3781-156_3781-155delinsCT	ENSP00000497203.1:n.3781-156_3781-155delinsCT
ENST00000685018.2:c.*177-156_*177-155delinsCT	ENSP00000510194.2:n.*177-156_*177-155delinsCT
ENST00000687278.2:c.*617-156_*617-155delinsCT	ENSP00000509593.2:n.*617-156_*617-155delinsCT
ENST00000699585.1:c.*173-156_*173-155delinsCT	ENSP00000514456.1:n.*173-156_*173-155delinsCT
ENST00000699598.1:c.3964-156_3964-155delinsCT	ENSP00000514467.1:n.3964-156_3964-155delinsCT
ENST00000699599.1:c.*177-156_*177-155delinsCT	ENSP00000514468.1:n.*177-156_*177-155delinsCT
ENST00000699600.1:c.*625-156_*625-155delinsCT	ENSP00000514469.1:n.*625-156_*625-155delinsCT
ENST00000699601.1:c.*2339-156_*2339-155delinsCT	ENSP00000514470.1:n.*2339-156_*2339-155delinsCT
ENST00000699602.1:c.3958-156_3958-155delinsCT	ENSP00000514471.1:n.3958-156_3958-155delinsCT
ENST00000699604.1:c.*3788-156_*3788-155delinsCT	ENSP00000514472.1:n.*3788-156_*3788-155delinsCT
ENST00000699605.1:c.3538-156_3538-155delinsCT	ENSP00000514473.1:n.3538-156_3538-155delinsCT
ENST00000699606.1:n.2132-156_2132-155delinsCT
ENST00000685018.1:c.828-156_828-155delinsCT	ENSP00000510194.1:n.828-156_828-155delinsCT
ENST00000687278.1:c.1751-156_1751-155delinsCT	ENSP00000509593.1:n.1751-156_1751-155delinsCT
ENST00000689011.1:c.546-156_546-155delinsCT
ENST00000003084.11:c.3964-156_3964-155delinsCT MANE Select	ENSP00000003084.6:n.3964-156_3964-155delinsCT
ENST00000647720.1:c.1414-156_1414-155delinsCT
ENST00000649781.1:c.3781-156_3781-155delinsCT	ENSP00000497203.1:n.3781-156_3781-155delinsCT
ENST00000003084.10:c.3964-156_3964-155delinsCT	ENSP00000003084.6:n.3964-156_3964-155delinsCT
ENST00000426809.5:c.3874-156_3874-155delinsCT	ENSP00000389119.1:n.3874-156_3874-155delinsCT
ENST00000600166.1:c.90-156_90-155delinsCT
NM_000492.3:c.3964-156_3964-155delinsCT , LRG_663t1:c.3964-156_3964-155delinsCT	NP_000483.3:n.3964-156_3964-155delinsCT
XM_011515751.1:c.4054-156_4054-155delinsCT	XP_011514053.1:n.4054-156_4054-155delinsCT
XM_011515752.1:c.4054-156_4054-155delinsCT	XP_011514054.1:n.4054-156_4054-155delinsCT
XM_011515753.1:c.3721-156_3721-155delinsCT	XP_011514055.1:n.3721-156_3721-155delinsCT
XM_011515754.1:c.3721-156_3721-155delinsCT	XP_011514056.1:n.3721-156_3721-155delinsCT
NM_000492.4:c.3964-156_3964-155delinsCT MANE Select	NP_000483.3:n.3964-156_3964-155delinsCT