Canonical Allele Identifier: CA913111908
Gene: CFTR HGNC NCBI
CFTR-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.117199719dup (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117559665dup , CM000669.2:g.117559665dup GRCh38
NC_000007.13:g.117199719dup , CM000669.1:g.117199719dup GRCh37
NC_000007.12:g.116986955dup NCBI36
NG_016465.4:g.98882dup , LRG_663:g.98882dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.1584+10dup (CFTR) ENSP00000497673.2:n.1584+10dup
ENST00000647978.2:c.*1298+10dup (CFTR) ENSP00000497658.1:n.*1298+10dup
ENST00000649781.2:c.1401+10dup (CFTR) ENSP00000497203.1:n.1401+10dup
ENST00000685018.2:c.1584+10dup (CFTR) ENSP00000510194.2:n.1584+10dup
ENST00000687278.2:c.1584+10dup (CFTR) ENSP00000509593.2:n.1584+10dup
ENST00000699585.1:c.1584+10dup (CFTR) ENSP00000514456.1:n.1584+10dup
ENST00000699596.1:c.1594dup (CFTR) ENSP00000514465.1:p.Tyr532LeufsTer?
ENST00000699597.1:c.*152dup (CFTR) ENSP00000514466.1:n.*152dup
ENST00000699598.1:c.1584+10dup (CFTR) ENSP00000514467.1:n.1584+10dup
ENST00000699599.1:c.1584+10dup (CFTR) ENSP00000514468.1:n.1584+10dup
ENST00000699600.1:c.1584+10dup (CFTR) ENSP00000514469.1:n.1584+10dup
ENST00000699601.1:c.1584+10dup (CFTR) ENSP00000514470.1:n.1584+10dup
ENST00000699602.1:c.1584+10dup (CFTR) ENSP00000514471.1:n.1584+10dup
ENST00000699604.1:c.*1408+10dup (CFTR) ENSP00000514472.1:n.*1408+10dup
ENST00000699605.1:c.1158+10dup (CFTR) ENSP00000514473.1:n.1158+10dup
ENST00000003084.11:c.1584+10dup (CFTR) MANE Select ENSP00000003084.6:n.1584+10dup
ENST00000647978.1:c.*1298+10dup (CFTR) ENSP00000497658.1:n.*1298+10dup
ENST00000648260.1:c.1401+10dup (CFTR) ENSP00000497957.1:n.1401+10dup
ENST00000649406.1:c.1401+10dup (CFTR) ENSP00000497965.1:n.1401+10dup
ENST00000649781.1:c.1401+10dup (CFTR) ENSP00000497203.1:n.1401+10dup
ENST00000003084.10:c.1584+10dup (CFTR) ENSP00000003084.6:n.1584+10dup
ENST00000426809.5:c.1494+10dup (CFTR) ENSP00000389119.1:n.1494+10dup
ENST00000472848.1:n.18+10dup (CFTR)
NM_000492.3:c.1584+10dup , LRG_663t1:c.1584+10dup (CFTR) NP_000483.3:n.1584+10dup
XM_011515751.1:c.1674+10dup (CFTR) XP_011514053.1:n.1674+10dup
XM_011515752.1:c.1674+10dup (CFTR) XP_011514054.1:n.1674+10dup
XM_011515753.1:c.1341+10dup (CFTR) XP_011514055.1:n.1341+10dup
XM_011515754.1:c.1341+10dup (CFTR) XP_011514056.1:n.1341+10dup
NR_149084.1:n.221+1068dup (CFTR-AS1)
NM_000492.4:c.1584+10dup (CFTR) MANE Select NP_000483.3:n.1584+10dup