Canonical Allele Identifier: CA164960406
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 973860
ClinVar RCV Id: RCV001250518
dbSNP Id: rs936934088

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117603780C>T , CM000669.2:g.117603780C>T GRCh38
NC_000007.13:g.117243834C>T , CM000669.1:g.117243834C>T GRCh37
NC_000007.12:g.117031070C>T NCBI36
NG_016465.4:g.142997C>T , LRG_663:g.142997C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.2906C>T ENSP00000497673.2:p.Ala969Val
ENST00000647978.2:c.*2620C>T ENSP00000497658.1:n.*2620C>T
ENST00000649781.2:c.2723C>T ENSP00000497203.1:p.Ala908Val
ENST00000685018.2:c.2906C>T ENSP00000510194.2:p.Ala969Val
ENST00000687278.2:c.2906C>T ENSP00000509593.2:p.Ala969Val
ENST00000699585.1:c.2906C>T ENSP00000514456.1:p.Ala969Val
ENST00000699598.1:c.2906C>T ENSP00000514467.1:p.Ala969Val
ENST00000699599.1:c.2906C>T ENSP00000514468.1:p.Ala969Val
ENST00000699600.1:c.2906C>T ENSP00000514469.1:p.Ala969Val
ENST00000699601.1:c.*1206C>T ENSP00000514470.1:n.*1206C>T
ENST00000699602.1:c.2906C>T ENSP00000514471.1:p.Ala969Val
ENST00000699604.1:c.*2730C>T ENSP00000514472.1:n.*2730C>T
ENST00000699605.1:c.2480C>T ENSP00000514473.1:p.Ala827Val
ENST00000687278.1:c.497C>T ENSP00000509593.1:p.Ala166Val
ENST00000003084.11:c.2906C>T MANE Select ENSP00000003084.6:p.Ala969Val
ENST00000647720.1:c.556C>T
ENST00000648260.1:c.1688C>T ENSP00000497957.1:p.Ala563Val
ENST00000649406.1:c.2723C>T ENSP00000497965.1:p.Ala908Val
ENST00000649781.1:c.2723C>T ENSP00000497203.1:p.Ala908Val
ENST00000003084.10:c.2906C>T ENSP00000003084.6:p.Ala969Val
ENST00000426809.5:c.2816C>T ENSP00000389119.1:p.Ala939Val
NM_000492.3:c.2906C>T , LRG_663t1:c.2906C>T NP_000483.3:p.Ala969Val
XM_011515751.1:c.2996C>T XP_011514053.1:p.Ala999Val
XM_011515752.1:c.2996C>T XP_011514054.1:p.Ala999Val
XM_011515753.1:c.2663C>T XP_011514055.1:p.Ala888Val
XM_011515754.1:c.2663C>T XP_011514056.1:p.Ala888Val
NM_000492.4:c.2906C>T MANE Select NP_000483.3:p.Ala969Val