Canonical Allele Identifier: CA368993550
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117614670C>G , CM000669.2:g.117614670C>G GRCh38
NC_000007.13:g.117254724C>G , CM000669.1:g.117254724C>G GRCh37
NC_000007.12:g.117041960C>G NCBI36
NG_016465.4:g.153887C>G , LRG_663:g.153887C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.3425C>G ENSP00000497673.2:p.Thr1142Arg
ENST00000647978.2:c.*3139C>G ENSP00000497658.1:n.*3139C>G
ENST00000649781.2:c.3242C>G ENSP00000497203.1:p.Thr1081Arg
ENST00000685018.2:c.3425C>G ENSP00000510194.2:p.Thr1142Arg
ENST00000687278.2:c.3425C>G ENSP00000509593.2:p.Thr1142Arg
ENST00000699585.1:c.3425C>G ENSP00000514456.1:p.Thr1142Arg
ENST00000699598.1:c.3425C>G ENSP00000514467.1:p.Thr1142Arg
ENST00000699599.1:c.3425C>G ENSP00000514468.1:p.Thr1142Arg
ENST00000699600.1:c.3425C>G ENSP00000514469.1:p.Thr1142Arg
ENST00000699601.1:c.*1800C>G ENSP00000514470.1:n.*1800C>G
ENST00000699602.1:c.3419C>G ENSP00000514471.1:p.Thr1140Arg
ENST00000699604.1:c.*3249C>G ENSP00000514472.1:n.*3249C>G
ENST00000699605.1:c.2999C>G ENSP00000514473.1:p.Thr1000Arg
ENST00000685018.1:c.173C>G ENSP00000510194.1:p.Thr58Arg
ENST00000687278.1:c.1016C>G ENSP00000509593.1:p.Thr339Arg
ENST00000689011.1:c.7C>G
ENST00000003084.11:c.3425C>G MANE Select ENSP00000003084.6:p.Thr1142Arg
ENST00000647720.1:c.1075C>G
ENST00000648260.1:c.2207C>G ENSP00000497957.1:p.Thr736Arg
ENST00000649406.1:c.3242C>G ENSP00000497965.1:p.Thr1081Arg
ENST00000649781.1:c.3242C>G ENSP00000497203.1:p.Thr1081Arg
ENST00000003084.10:c.3425C>G ENSP00000003084.6:p.Thr1142Arg
ENST00000426809.5:c.3335C>G ENSP00000389119.1:p.Thr1112Arg
ENST00000468795.1:c.250C>G
NM_000492.3:c.3425C>G , LRG_663t1:c.3425C>G NP_000483.3:p.Thr1142Arg
XM_011515751.1:c.3515C>G XP_011514053.1:p.Thr1172Arg
XM_011515752.1:c.3515C>G XP_011514054.1:p.Thr1172Arg
XM_011515753.1:c.3182C>G XP_011514055.1:p.Thr1061Arg
XM_011515754.1:c.3182C>G XP_011514056.1:p.Thr1061Arg
NM_000492.4:c.3425C>G MANE Select NP_000483.3:p.Thr1142Arg