Canonical Allele Identifier: CA1737340839
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117509223G= , CM000669.2:g.117509223G= GRCh38
NC_000007.13:g.117149277G= , CM000669.1:g.117149277G= GRCh37
NC_000007.12:g.116936513G= NCBI36
NG_016465.4:g.48440G= , LRG_663:g.48440G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.273+81G= ENSP00000497673.2:n.273+81G=
ENST00000647978.2:c.*170+81G= ENSP00000497658.1:n.*170+81G=
ENST00000649781.2:c.273+81G= ENSP00000497203.1:n.273+81G=
ENST00000649850.2:c.*251G= ENSP00000514457.1:n.*251G=
ENST00000685018.2:c.273+81G= ENSP00000510194.2:n.273+81G=
ENST00000687278.2:c.273+81G= ENSP00000509593.2:n.273+81G=
ENST00000699585.1:c.273+81G= ENSP00000514456.1:n.273+81G=
ENST00000699596.1:c.273+81G= ENSP00000514465.1:n.273+81G=
ENST00000699597.1:c.273+81G= ENSP00000514466.1:n.273+81G=
ENST00000699598.1:c.273+81G= ENSP00000514467.1:n.273+81G=
ENST00000699599.1:c.273+81G= ENSP00000514468.1:n.273+81G=
ENST00000699600.1:c.273+81G= ENSP00000514469.1:n.273+81G=
ENST00000699601.1:c.273+81G= ENSP00000514470.1:n.273+81G=
ENST00000699602.1:c.273+81G= ENSP00000514471.1:n.273+81G=
ENST00000699604.1:c.*97+81G= ENSP00000514472.1:n.*97+81G=
ENST00000699605.1:c.30+81G= ENSP00000514473.1:n.30+81G=
ENST00000446805.2:c.30+81G= ENSP00000417012.1:n.30+81G=
ENST00000003084.11:c.273+81G= MANE Select ENSP00000003084.6:n.273+81G=
ENST00000647639.1:n.357+81G=
ENST00000647978.1:c.*170+81G= ENSP00000497658.1:n.*170+81G=
ENST00000648260.1:c.273+81G= ENSP00000497957.1:n.273+81G=
ENST00000649406.1:c.273+81G= ENSP00000497965.1:n.273+81G=
ENST00000649781.1:c.273+81G= ENSP00000497203.1:n.273+81G=
ENST00000649850.1:n.511G=
ENST00000673785.1:c.30+81G= ENSP00000501235.1:n.30+81G=
ENST00000003084.10:c.273+81G= ENSP00000003084.6:n.273+81G=
ENST00000426809.5:c.273+81G= ENSP00000389119.1:n.273+81G=
ENST00000446805.1:c.30+81G= ENSP00000417012.1:n.30+81G=
NM_000492.3:c.273+81G= , LRG_663t1:c.273+81G= NP_000483.3:n.273+81G=
XM_011515751.1:c.363+81G= XP_011514053.1:n.363+81G=
XM_011515752.1:c.363+81G= XP_011514054.1:n.363+81G=
XM_011515753.1:c.30+81G= XP_011514055.1:n.30+81G=
XM_011515754.1:c.30+81G= XP_011514056.1:n.30+81G=
NM_000492.4:c.273+81G= MANE Select NP_000483.3:n.273+81G=