Canonical Allele Identifier: CA368986500

Gene: CFTR

Linked Data

• gnomAD v4: 7-117603592-T-G
• MyVariant Identifiers: chr7:g.117243646T>G (hg19) ; chr7:g.117603592T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603592T>G , CM000669.2:g.117603592T>G	GRCh38
NC_000007.13:g.117243646T>G , CM000669.1:g.117243646T>G	GRCh37
NC_000007.12:g.117030882T>G	NCBI36
NG_016465.4:g.142809T>G , LRG_663:g.142809T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2718T>G	ENSP00000497673.2:p.Ile906Met
ENST00000647978.2:c.*2432T>G	ENSP00000497658.1:n.*2432T>G
ENST00000649781.2:c.2535T>G	ENSP00000497203.1:p.Ile845Met
ENST00000685018.2:c.2718T>G	ENSP00000510194.2:p.Ile906Met
ENST00000687278.2:c.2718T>G	ENSP00000509593.2:p.Ile906Met
ENST00000699585.1:c.2718T>G	ENSP00000514456.1:p.Ile906Met
ENST00000699598.1:c.2718T>G	ENSP00000514467.1:p.Ile906Met
ENST00000699599.1:c.2718T>G	ENSP00000514468.1:p.Ile906Met
ENST00000699600.1:c.2718T>G	ENSP00000514469.1:p.Ile906Met
ENST00000699601.1:c.*1018T>G	ENSP00000514470.1:n.*1018T>G
ENST00000699602.1:c.2718T>G	ENSP00000514471.1:p.Ile906Met
ENST00000699604.1:c.*2542T>G	ENSP00000514472.1:n.*2542T>G
ENST00000699605.1:c.2292T>G	ENSP00000514473.1:p.Ile764Met
ENST00000687278.1:c.309T>G	ENSP00000509593.1:p.Ile103Met
ENST00000003084.11:c.2718T>G MANE Select	ENSP00000003084.6:p.Ile906Met
ENST00000647720.1:c.368T>G
ENST00000648260.1:c.1500T>G	ENSP00000497957.1:p.Ile500Met
ENST00000649406.1:c.2535T>G	ENSP00000497965.1:p.Ile845Met
ENST00000649781.1:c.2535T>G	ENSP00000497203.1:p.Ile845Met
ENST00000003084.10:c.2718T>G	ENSP00000003084.6:p.Ile906Met
ENST00000426809.5:c.2628T>G	ENSP00000389119.1:p.Ile876Met
NM_000492.3:c.2718T>G , LRG_663t1:c.2718T>G	NP_000483.3:p.Ile906Met
XM_011515751.1:c.2808T>G	XP_011514053.1:p.Ile936Met
XM_011515752.1:c.2808T>G	XP_011514054.1:p.Ile936Met
XM_011515753.1:c.2475T>G	XP_011514055.1:p.Ile825Met
XM_011515754.1:c.2475T>G	XP_011514056.1:p.Ile825Met
NM_000492.4:c.2718T>G MANE Select	NP_000483.3:p.Ile906Met