Canonical Allele Identifier: CA368983792

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117234990T>A (hg19) ; chr7:g.117594936T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117594936T>A , CM000669.2:g.117594936T>A	GRCh38
NC_000007.13:g.117234990T>A , CM000669.1:g.117234990T>A	GRCh37
NC_000007.12:g.117022226T>A	NCBI36
NG_016465.4:g.134153T>A , LRG_663:g.134153T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2497T>A	ENSP00000497673.2:p.Phe833Ile
ENST00000647978.2:c.*2211T>A	ENSP00000497658.1:n.*2211T>A
ENST00000649781.2:c.2314T>A	ENSP00000497203.1:p.Phe772Ile
ENST00000685018.2:c.2497T>A	ENSP00000510194.2:p.Phe833Ile
ENST00000687278.2:c.2497T>A	ENSP00000509593.2:p.Phe833Ile
ENST00000699585.1:c.2497T>A	ENSP00000514456.1:p.Phe833Ile
ENST00000699598.1:c.2497T>A	ENSP00000514467.1:p.Phe833Ile
ENST00000699599.1:c.2497T>A	ENSP00000514468.1:p.Phe833Ile
ENST00000699600.1:c.2497T>A	ENSP00000514469.1:p.Phe833Ile
ENST00000699601.1:c.*797T>A	ENSP00000514470.1:n.*797T>A
ENST00000699602.1:c.2497T>A	ENSP00000514471.1:p.Phe833Ile
ENST00000699604.1:c.*2321T>A	ENSP00000514472.1:n.*2321T>A
ENST00000699605.1:c.2071T>A	ENSP00000514473.1:p.Phe691Ile
ENST00000687278.1:c.88T>A	ENSP00000509593.1:p.Phe30Ile
ENST00000003084.11:c.2497T>A MANE Select	ENSP00000003084.6:p.Phe833Ile
ENST00000647720.1:c.147T>A
ENST00000647978.1:c.*2211T>A	ENSP00000497658.1:n.*2211T>A
ENST00000648260.1:c.1402-7890T>A	ENSP00000497957.1:n.1402-7890T>A
ENST00000649406.1:c.2314T>A	ENSP00000497965.1:p.Phe772Ile
ENST00000649781.1:c.2314T>A	ENSP00000497203.1:p.Phe772Ile
ENST00000003084.10:c.2497T>A	ENSP00000003084.6:p.Phe833Ile
ENST00000426809.5:c.2407T>A	ENSP00000389119.1:p.Phe803Ile
NM_000492.3:c.2497T>A , LRG_663t1:c.2497T>A	NP_000483.3:p.Phe833Ile
XM_011515751.1:c.2587T>A	XP_011514053.1:p.Phe863Ile
XM_011515752.1:c.2587T>A	XP_011514054.1:p.Phe863Ile
XM_011515753.1:c.2254T>A	XP_011514055.1:p.Phe752Ile
XM_011515754.1:c.2254T>A	XP_011514056.1:p.Phe752Ile
NM_000492.4:c.2497T>A MANE Select	NP_000483.3:p.Phe833Ile