Canonical Allele Identifier: CA368983813
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117594940T>C , CM000669.2:g.117594940T>C GRCh38
NC_000007.13:g.117234994T>C , CM000669.1:g.117234994T>C GRCh37
NC_000007.12:g.117022230T>C NCBI36
NG_016465.4:g.134157T>C , LRG_663:g.134157T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.2501T>C ENSP00000497673.2:p.Phe834Ser
ENST00000647978.2:c.*2215T>C ENSP00000497658.1:n.*2215T>C
ENST00000649781.2:c.2318T>C ENSP00000497203.1:p.Phe773Ser
ENST00000685018.2:c.2501T>C ENSP00000510194.2:p.Phe834Ser
ENST00000687278.2:c.2501T>C ENSP00000509593.2:p.Phe834Ser
ENST00000699585.1:c.2501T>C ENSP00000514456.1:p.Phe834Ser
ENST00000699598.1:c.2501T>C ENSP00000514467.1:p.Phe834Ser
ENST00000699599.1:c.2501T>C ENSP00000514468.1:p.Phe834Ser
ENST00000699600.1:c.2501T>C ENSP00000514469.1:p.Phe834Ser
ENST00000699601.1:c.*801T>C ENSP00000514470.1:n.*801T>C
ENST00000699602.1:c.2501T>C ENSP00000514471.1:p.Phe834Ser
ENST00000699604.1:c.*2325T>C ENSP00000514472.1:n.*2325T>C
ENST00000699605.1:c.2075T>C ENSP00000514473.1:p.Phe692Ser
ENST00000687278.1:c.92T>C ENSP00000509593.1:p.Phe31Ser
ENST00000003084.11:c.2501T>C MANE Select ENSP00000003084.6:p.Phe834Ser
ENST00000647720.1:c.151T>C
ENST00000647978.1:c.*2215T>C ENSP00000497658.1:n.*2215T>C
ENST00000648260.1:c.1402-7886T>C ENSP00000497957.1:n.1402-7886T>C
ENST00000649406.1:c.2318T>C ENSP00000497965.1:p.Phe773Ser
ENST00000649781.1:c.2318T>C ENSP00000497203.1:p.Phe773Ser
ENST00000003084.10:c.2501T>C ENSP00000003084.6:p.Phe834Ser
ENST00000426809.5:c.2411T>C ENSP00000389119.1:p.Phe804Ser
NM_000492.3:c.2501T>C , LRG_663t1:c.2501T>C NP_000483.3:p.Phe834Ser
XM_011515751.1:c.2591T>C XP_011514053.1:p.Phe864Ser
XM_011515752.1:c.2591T>C XP_011514054.1:p.Phe864Ser
XM_011515753.1:c.2258T>C XP_011514055.1:p.Phe753Ser
XM_011515754.1:c.2258T>C XP_011514056.1:p.Phe753Ser
NM_000492.4:c.2501T>C MANE Select NP_000483.3:p.Phe834Ser