Canonical Allele Identifier: CA368984510
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 555210
ClinVar RCV Id: RCV000670985
dbSNP Id: rs1800135

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117666937C>A , CM000669.2:g.117666937C>A GRCh38
NC_000007.13:g.117306991C>A , CM000669.1:g.117306991C>A GRCh37
NC_000007.12:g.117094227C>A NCBI36
NG_016465.4:g.206154C>A , LRG_663:g.206154C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.*481C>A ENSP00000497673.2:n.*481C>A
ENST00000647978.2:c.*3986C>A ENSP00000497658.1:n.*3986C>A
ENST00000649781.2:c.4089C>A ENSP00000497203.1:p.Tyr1363Ter
ENST00000685018.2:c.*485C>A ENSP00000510194.2:n.*485C>A
ENST00000687278.2:c.*896-665C>A ENSP00000509593.2:n.*896-665C>A
ENST00000699585.1:c.*741C>A ENSP00000514456.1:n.*741C>A
ENST00000699598.1:c.4265C>A ENSP00000514467.1:p.Thr1422Lys
ENST00000699599.1:c.*485C>A ENSP00000514468.1:n.*485C>A
ENST00000699600.1:c.*904-665C>A ENSP00000514469.1:n.*904-665C>A
ENST00000699601.1:c.*2647C>A ENSP00000514470.1:n.*2647C>A
ENST00000699602.1:c.4266C>A ENSP00000514471.1:p.Tyr1422Ter
ENST00000699604.1:c.*4096C>A ENSP00000514472.1:n.*4096C>A
ENST00000699605.1:c.3846C>A ENSP00000514473.1:p.Tyr1282Ter
ENST00000699606.1:n.3783C>A
ENST00000685018.1:c.1136C>A ENSP00000510194.1:n.1136C>A
ENST00000687278.1:c.2030-665C>A ENSP00000509593.1:n.2030-665C>A
ENST00000689011.1:c.1114C>A
ENST00000003084.11:c.4272C>A MANE Select ENSP00000003084.6:p.Tyr1424Ter
ENST00000647720.1:c.1722C>A
ENST00000649781.1:c.4089C>A ENSP00000497203.1:p.Tyr1363Ter
ENST00000003084.10:c.4272C>A ENSP00000003084.6:p.Tyr1424Ter
ENST00000426809.5:c.4182C>A ENSP00000389119.1:p.Tyr1394Ter
ENST00000600166.1:c.368+1373C>A
NM_000492.3:c.4272C>A , LRG_663t1:c.4272C>A NP_000483.3:p.Tyr1424Ter
XM_011515751.1:c.4362C>A XP_011514053.1:p.Tyr1454Ter
XM_011515753.1:c.4029C>A XP_011514055.1:p.Tyr1343Ter
XM_011515754.1:c.4029C>A XP_011514056.1:p.Tyr1343Ter
NM_000492.4:c.4272C>A MANE Select NP_000483.3:p.Tyr1424Ter