Canonical Allele Identifier: CA368986413

Gene: CFTR

Linked Data

• COSMIC: COSM4445079
• MyVariant Identifiers: chr7:g.117243606G>T (hg19) ; chr7:g.117603552G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603552G>T , CM000669.2:g.117603552G>T	GRCh38
NC_000007.13:g.117243606G>T , CM000669.1:g.117243606G>T	GRCh37
NC_000007.12:g.117030842G>T	NCBI36
NG_016465.4:g.142769G>T , LRG_663:g.142769G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2678G>T	ENSP00000497673.2:p.Gly893Val
ENST00000647978.2:c.*2392G>T	ENSP00000497658.1:n.*2392G>T
ENST00000649781.2:c.2495G>T	ENSP00000497203.1:p.Gly832Val
ENST00000685018.2:c.2678G>T	ENSP00000510194.2:p.Gly893Val
ENST00000687278.2:c.2678G>T	ENSP00000509593.2:p.Gly893Val
ENST00000699585.1:c.2678G>T	ENSP00000514456.1:p.Gly893Val
ENST00000699598.1:c.2678G>T	ENSP00000514467.1:p.Gly893Val
ENST00000699599.1:c.2678G>T	ENSP00000514468.1:p.Gly893Val
ENST00000699600.1:c.2678G>T	ENSP00000514469.1:p.Gly893Val
ENST00000699601.1:c.*978G>T	ENSP00000514470.1:n.*978G>T
ENST00000699602.1:c.2678G>T	ENSP00000514471.1:p.Gly893Val
ENST00000699604.1:c.*2502G>T	ENSP00000514472.1:n.*2502G>T
ENST00000699605.1:c.2252G>T	ENSP00000514473.1:p.Gly751Val
ENST00000687278.1:c.269G>T	ENSP00000509593.1:p.Gly90Val
ENST00000003084.11:c.2678G>T MANE Select	ENSP00000003084.6:p.Gly893Val
ENST00000647720.1:c.328G>T
ENST00000648260.1:c.1460G>T	ENSP00000497957.1:p.Gly487Val
ENST00000649406.1:c.2495G>T	ENSP00000497965.1:p.Gly832Val
ENST00000649781.1:c.2495G>T	ENSP00000497203.1:p.Gly832Val
ENST00000003084.10:c.2678G>T	ENSP00000003084.6:p.Gly893Val
ENST00000426809.5:c.2588G>T	ENSP00000389119.1:p.Gly863Val
NM_000492.3:c.2678G>T , LRG_663t1:c.2678G>T	NP_000483.3:p.Gly893Val
XM_011515751.1:c.2768G>T	XP_011514053.1:p.Gly923Val
XM_011515752.1:c.2768G>T	XP_011514054.1:p.Gly923Val
XM_011515753.1:c.2435G>T	XP_011514055.1:p.Gly812Val
XM_011515754.1:c.2435G>T	XP_011514056.1:p.Gly812Val
NM_000492.4:c.2678G>T MANE Select	NP_000483.3:p.Gly893Val