Canonical Allele Identifier: CA326911

Gene: CFTR

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603624A>G , CM000669.2:g.117603624A>G	GRCh38
NC_000007.13:g.117243678A>G , CM000669.1:g.117243678A>G	GRCh37
NC_000007.12:g.117030914A>G	NCBI36
NG_016465.4:g.142841A>G , LRG_663:g.142841A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2750A>G	ENSP00000497673.2:p.Tyr917Cys
ENST00000647978.2:c.*2464A>G	ENSP00000497658.1:n.*2464A>G
ENST00000649781.2:c.2567A>G	ENSP00000497203.1:p.Tyr856Cys
ENST00000685018.2:c.2750A>G	ENSP00000510194.2:p.Tyr917Cys
ENST00000687278.2:c.2750A>G	ENSP00000509593.2:p.Tyr917Cys
ENST00000699585.1:c.2750A>G	ENSP00000514456.1:p.Tyr917Cys
ENST00000699598.1:c.2750A>G	ENSP00000514467.1:p.Tyr917Cys
ENST00000699599.1:c.2750A>G	ENSP00000514468.1:p.Tyr917Cys
ENST00000699600.1:c.2750A>G	ENSP00000514469.1:p.Tyr917Cys
ENST00000699601.1:c.*1050A>G	ENSP00000514470.1:n.*1050A>G
ENST00000699602.1:c.2750A>G	ENSP00000514471.1:p.Tyr917Cys
ENST00000699604.1:c.*2574A>G	ENSP00000514472.1:n.*2574A>G
ENST00000699605.1:c.2324A>G	ENSP00000514473.1:p.Tyr775Cys
ENST00000687278.1:c.341A>G	ENSP00000509593.1:p.Tyr114Cys
ENST00000003084.11:c.2750A>G MANE Select	ENSP00000003084.6:p.Tyr917Cys
ENST00000647720.1:c.400A>G
ENST00000648260.1:c.1532A>G	ENSP00000497957.1:p.Tyr511Cys
ENST00000649406.1:c.2567A>G	ENSP00000497965.1:p.Tyr856Cys
ENST00000649781.1:c.2567A>G	ENSP00000497203.1:p.Tyr856Cys
ENST00000003084.10:c.2750A>G	ENSP00000003084.6:p.Tyr917Cys
ENST00000426809.5:c.2660A>G	ENSP00000389119.1:p.Tyr887Cys
NM_000492.3:c.2750A>G , LRG_663t1:c.2750A>G	NP_000483.3:p.Tyr917Cys
XM_011515751.1:c.2840A>G	XP_011514053.1:p.Tyr947Cys
XM_011515752.1:c.2840A>G	XP_011514054.1:p.Tyr947Cys
XM_011515753.1:c.2507A>G	XP_011514055.1:p.Tyr836Cys
XM_011515754.1:c.2507A>G	XP_011514056.1:p.Tyr836Cys
NM_000492.4:c.2750A>G MANE Select	NP_000483.3:p.Tyr917Cys