Canonical Allele Identifier: CA368986791

Gene: CFTR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603654T>A , CM000669.2:g.117603654T>A	GRCh38
NC_000007.13:g.117243708T>A , CM000669.1:g.117243708T>A	GRCh37
NC_000007.12:g.117030944T>A	NCBI36
NG_016465.4:g.142871T>A , LRG_663:g.142871T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2780T>A	ENSP00000497673.2:p.Leu927His
ENST00000647978.2:c.*2494T>A	ENSP00000497658.1:n.*2494T>A
ENST00000649781.2:c.2597T>A	ENSP00000497203.1:p.Leu866His
ENST00000685018.2:c.2780T>A	ENSP00000510194.2:p.Leu927His
ENST00000687278.2:c.2780T>A	ENSP00000509593.2:p.Leu927His
ENST00000699585.1:c.2780T>A	ENSP00000514456.1:p.Leu927His
ENST00000699598.1:c.2780T>A	ENSP00000514467.1:p.Leu927His
ENST00000699599.1:c.2780T>A	ENSP00000514468.1:p.Leu927His
ENST00000699600.1:c.2780T>A	ENSP00000514469.1:p.Leu927His
ENST00000699601.1:c.*1080T>A	ENSP00000514470.1:n.*1080T>A
ENST00000699602.1:c.2780T>A	ENSP00000514471.1:p.Leu927His
ENST00000699604.1:c.*2604T>A	ENSP00000514472.1:n.*2604T>A
ENST00000699605.1:c.2354T>A	ENSP00000514473.1:p.Leu785His
ENST00000687278.1:c.371T>A	ENSP00000509593.1:p.Leu124His
ENST00000003084.11:c.2780T>A MANE Select	ENSP00000003084.6:p.Leu927His
ENST00000647720.1:c.430T>A
ENST00000648260.1:c.1562T>A	ENSP00000497957.1:p.Leu521His
ENST00000649406.1:c.2597T>A	ENSP00000497965.1:p.Leu866His
ENST00000649781.1:c.2597T>A	ENSP00000497203.1:p.Leu866His
ENST00000003084.10:c.2780T>A	ENSP00000003084.6:p.Leu927His
ENST00000426809.5:c.2690T>A	ENSP00000389119.1:p.Leu897His
NM_000492.3:c.2780T>A , LRG_663t1:c.2780T>A	NP_000483.3:p.Leu927His
XM_011515751.1:c.2870T>A	XP_011514053.1:p.Leu957His
XM_011515752.1:c.2870T>A	XP_011514054.1:p.Leu957His
XM_011515753.1:c.2537T>A	XP_011514055.1:p.Leu846His
XM_011515754.1:c.2537T>A	XP_011514056.1:p.Leu846His
NM_000492.4:c.2780T>A MANE Select	NP_000483.3:p.Leu927His