Canonical Allele Identifier: CA368989085

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117246764T>G (hg19) ; chr7:g.117606710T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117606710T>G , CM000669.2:g.117606710T>G	GRCh38
NC_000007.13:g.117246764T>G , CM000669.1:g.117246764T>G	GRCh37
NC_000007.12:g.117034000T>G	NCBI36
NG_016465.4:g.145927T>G , LRG_663:g.145927T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2945T>G	ENSP00000497673.2:p.Ile982Ser
ENST00000647978.2:c.*2659T>G	ENSP00000497658.1:n.*2659T>G
ENST00000649781.2:c.2762T>G	ENSP00000497203.1:p.Ile921Ser
ENST00000685018.2:c.2945T>G	ENSP00000510194.2:p.Ile982Ser
ENST00000687278.2:c.2945T>G	ENSP00000509593.2:p.Ile982Ser
ENST00000699585.1:c.2945T>G	ENSP00000514456.1:p.Ile982Ser
ENST00000699598.1:c.2945T>G	ENSP00000514467.1:p.Ile982Ser
ENST00000699599.1:c.2945T>G	ENSP00000514468.1:p.Ile982Ser
ENST00000699600.1:c.2945T>G	ENSP00000514469.1:p.Ile982Ser
ENST00000699601.1:c.*1245T>G	ENSP00000514470.1:n.*1245T>G
ENST00000699602.1:c.2945T>G	ENSP00000514471.1:p.Ile982Ser
ENST00000699604.1:c.*2769T>G	ENSP00000514472.1:n.*2769T>G
ENST00000699605.1:c.2519T>G	ENSP00000514473.1:p.Ile840Ser
ENST00000687278.1:c.536T>G	ENSP00000509593.1:p.Ile179Ser
ENST00000003084.11:c.2945T>G MANE Select	ENSP00000003084.6:p.Ile982Ser
ENST00000647720.1:c.595T>G
ENST00000648260.1:c.1727T>G	ENSP00000497957.1:p.Ile576Ser
ENST00000649406.1:c.2762T>G	ENSP00000497965.1:p.Ile921Ser
ENST00000649781.1:c.2762T>G	ENSP00000497203.1:p.Ile921Ser
ENST00000003084.10:c.2945T>G	ENSP00000003084.6:p.Ile982Ser
ENST00000426809.5:c.2855T>G	ENSP00000389119.1:p.Ile952Ser
NM_000492.3:c.2945T>G , LRG_663t1:c.2945T>G	NP_000483.3:p.Ile982Ser
XM_011515751.1:c.3035T>G	XP_011514053.1:p.Ile1012Ser
XM_011515752.1:c.3035T>G	XP_011514054.1:p.Ile1012Ser
XM_011515753.1:c.2702T>G	XP_011514055.1:p.Ile901Ser
XM_011515754.1:c.2702T>G	XP_011514056.1:p.Ile901Ser
NM_000492.4:c.2945T>G MANE Select	NP_000483.3:p.Ile982Ser