Canonical Allele Identifier: CA368979002

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117232179T>A (hg19) ; chr7:g.117592125T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117592125T>A , CM000669.2:g.117592125T>A	GRCh38
NC_000007.13:g.117232179T>A , CM000669.1:g.117232179T>A	GRCh37
NC_000007.12:g.117019415T>A	NCBI36
NG_016465.4:g.131342T>A , LRG_663:g.131342T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.1958T>A	ENSP00000497673.2:p.Phe653Tyr
ENST00000647978.2:c.*1672T>A	ENSP00000497658.1:n.*1672T>A
ENST00000649781.2:c.1775T>A	ENSP00000497203.1:p.Phe592Tyr
ENST00000685018.2:c.1958T>A	ENSP00000510194.2:p.Phe653Tyr
ENST00000687278.2:c.1958T>A	ENSP00000509593.2:p.Phe653Tyr
ENST00000699585.1:c.1958T>A	ENSP00000514456.1:p.Phe653Tyr
ENST00000699598.1:c.1958T>A	ENSP00000514467.1:p.Phe653Tyr
ENST00000699599.1:c.1958T>A	ENSP00000514468.1:p.Phe653Tyr
ENST00000699600.1:c.1958T>A	ENSP00000514469.1:p.Phe653Tyr
ENST00000699601.1:c.*258T>A	ENSP00000514470.1:n.*258T>A
ENST00000699602.1:c.1958T>A	ENSP00000514471.1:p.Phe653Tyr
ENST00000699604.1:c.*1782T>A	ENSP00000514472.1:n.*1782T>A
ENST00000699605.1:c.1532T>A	ENSP00000514473.1:p.Phe511Tyr
ENST00000003084.11:c.1958T>A MANE Select	ENSP00000003084.6:p.Phe653Tyr
ENST00000647978.1:c.*1672T>A	ENSP00000497658.1:n.*1672T>A
ENST00000648260.1:c.1402-10701T>A	ENSP00000497957.1:n.1402-10701T>A
ENST00000649406.1:c.1775T>A	ENSP00000497965.1:p.Phe592Tyr
ENST00000649781.1:c.1775T>A	ENSP00000497203.1:p.Phe592Tyr
ENST00000003084.10:c.1958T>A	ENSP00000003084.6:p.Phe653Tyr
ENST00000426809.5:c.1868T>A	ENSP00000389119.1:p.Phe623Tyr
NM_000492.3:c.1958T>A , LRG_663t1:c.1958T>A	NP_000483.3:p.Phe653Tyr
XM_011515751.1:c.2048T>A	XP_011514053.1:p.Phe683Tyr
XM_011515752.1:c.2048T>A	XP_011514054.1:p.Phe683Tyr
XM_011515753.1:c.1715T>A	XP_011514055.1:p.Phe572Tyr
XM_011515754.1:c.1715T>A	XP_011514056.1:p.Phe572Tyr
NM_000492.4:c.1958T>A MANE Select	NP_000483.3:p.Phe653Tyr