Canonical Allele Identifier: CA368987166
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117603711A>C , CM000669.2:g.117603711A>C GRCh38
NC_000007.13:g.117243765A>C , CM000669.1:g.117243765A>C GRCh37
NC_000007.12:g.117031001A>C NCBI36
NG_016465.4:g.142928A>C , LRG_663:g.142928A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.2837A>C ENSP00000497673.2:p.Lys946Thr
ENST00000647978.2:c.*2551A>C ENSP00000497658.1:n.*2551A>C
ENST00000649781.2:c.2654A>C ENSP00000497203.1:p.Lys885Thr
ENST00000685018.2:c.2837A>C ENSP00000510194.2:p.Lys946Thr
ENST00000687278.2:c.2837A>C ENSP00000509593.2:p.Lys946Thr
ENST00000699585.1:c.2837A>C ENSP00000514456.1:p.Lys946Thr
ENST00000699598.1:c.2837A>C ENSP00000514467.1:p.Lys946Thr
ENST00000699599.1:c.2837A>C ENSP00000514468.1:p.Lys946Thr
ENST00000699600.1:c.2837A>C ENSP00000514469.1:p.Lys946Thr
ENST00000699601.1:c.*1137A>C ENSP00000514470.1:n.*1137A>C
ENST00000699602.1:c.2837A>C ENSP00000514471.1:p.Lys946Thr
ENST00000699604.1:c.*2661A>C ENSP00000514472.1:n.*2661A>C
ENST00000699605.1:c.2411A>C ENSP00000514473.1:p.Lys804Thr
ENST00000687278.1:c.428A>C ENSP00000509593.1:p.Lys143Thr
ENST00000003084.11:c.2837A>C MANE Select ENSP00000003084.6:p.Lys946Thr
ENST00000647720.1:c.487A>C
ENST00000648260.1:c.1619A>C ENSP00000497957.1:p.Lys540Thr
ENST00000649406.1:c.2654A>C ENSP00000497965.1:p.Lys885Thr
ENST00000649781.1:c.2654A>C ENSP00000497203.1:p.Lys885Thr
ENST00000003084.10:c.2837A>C ENSP00000003084.6:p.Lys946Thr
ENST00000426809.5:c.2747A>C ENSP00000389119.1:p.Lys916Thr
NM_000492.3:c.2837A>C , LRG_663t1:c.2837A>C NP_000483.3:p.Lys946Thr
XM_011515751.1:c.2927A>C XP_011514053.1:p.Lys976Thr
XM_011515752.1:c.2927A>C XP_011514054.1:p.Lys976Thr
XM_011515753.1:c.2594A>C XP_011514055.1:p.Lys865Thr
XM_011515754.1:c.2594A>C XP_011514056.1:p.Lys865Thr
NM_000492.4:c.2837A>C MANE Select NP_000483.3:p.Lys946Thr