Canonical Allele Identifier: CA368990234

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117250573T>A (hg19) ; chr7:g.117610519T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117610519T>A , CM000669.2:g.117610519T>A	GRCh38
NC_000007.13:g.117250573T>A , CM000669.1:g.117250573T>A	GRCh37
NC_000007.12:g.117037809T>A	NCBI36
NG_016465.4:g.149736T>A , LRG_663:g.149736T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.2989T>A	ENSP00000497673.2:p.Leu997Met
ENST00000647978.2:c.*2703T>A	ENSP00000497658.1:n.*2703T>A
ENST00000649781.2:c.2806T>A	ENSP00000497203.1:p.Leu936Met
ENST00000685018.2:c.2989T>A	ENSP00000510194.2:p.Leu997Met
ENST00000687278.2:c.2989T>A	ENSP00000509593.2:p.Leu997Met
ENST00000699585.1:c.2989T>A	ENSP00000514456.1:p.Leu997Met
ENST00000699598.1:c.2989T>A	ENSP00000514467.1:p.Leu997Met
ENST00000699599.1:c.2989T>A	ENSP00000514468.1:p.Leu997Met
ENST00000699600.1:c.2989T>A	ENSP00000514469.1:p.Leu997Met
ENST00000699601.1:c.*1289T>A	ENSP00000514470.1:n.*1289T>A
ENST00000699602.1:c.2989T>A	ENSP00000514471.1:p.Leu997Met
ENST00000699604.1:c.*2813T>A	ENSP00000514472.1:n.*2813T>A
ENST00000699605.1:c.2563T>A	ENSP00000514473.1:p.Leu855Met
ENST00000687278.1:c.580T>A	ENSP00000509593.1:p.Leu194Met
ENST00000003084.11:c.2989T>A MANE Select	ENSP00000003084.6:p.Leu997Met
ENST00000647720.1:c.639T>A
ENST00000648260.1:c.1771T>A	ENSP00000497957.1:p.Leu591Met
ENST00000649406.1:c.2806T>A	ENSP00000497965.1:p.Leu936Met
ENST00000649781.1:c.2806T>A	ENSP00000497203.1:p.Leu936Met
ENST00000003084.10:c.2989T>A	ENSP00000003084.6:p.Leu997Met
ENST00000426809.5:c.2899T>A	ENSP00000389119.1:p.Leu967Met
NM_000492.3:c.2989T>A , LRG_663t1:c.2989T>A	NP_000483.3:p.Leu997Met
XM_011515751.1:c.3079T>A	XP_011514053.1:p.Leu1027Met
XM_011515752.1:c.3079T>A	XP_011514054.1:p.Leu1027Met
XM_011515753.1:c.2746T>A	XP_011514055.1:p.Leu916Met
XM_011515754.1:c.2746T>A	XP_011514056.1:p.Leu916Met
NM_000492.4:c.2989T>A MANE Select	NP_000483.3:p.Leu997Met