Canonical Allele Identifier: CA1737384413
Gene: CFTR HGNC NCBI
CFTR-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117559547_117559549delinsTCA , CM000669.2:g.117559547_117559549delinsTCA GRCh38
NC_000007.13:g.117199601_117199603delinsTCA , CM000669.1:g.117199601_117199603delinsTCA GRCh37
NC_000007.12:g.116986837_116986839delinsTCA NCBI36
NG_016465.4:g.98764_98766delinsTCA , LRG_663:g.98764_98766delinsTCA

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.1476_1478delinsTCA (CFTR) ENSP00000497673.2:p.Ser492=
ENST00000647978.2:c.*1190_*1192delinsTCA (CFTR) ENSP00000497658.1:n.*1190_*1192delinsTCA
ENST00000649781.2:c.1293_1295delinsTCA (CFTR) ENSP00000497203.1:p.Ser431=
ENST00000685018.2:c.1476_1478delinsTCA (CFTR) ENSP00000510194.2:p.Ser492=
ENST00000687278.2:c.1476_1478delinsTCA (CFTR) ENSP00000509593.2:p.Ser492=
ENST00000699585.1:c.1476_1478delinsTCA (CFTR) ENSP00000514456.1:p.Ser492=
ENST00000699596.1:c.1476_1478delinsTCA (CFTR) ENSP00000514465.1:p.Ser492=
ENST00000699597.1:c.*34_*36delinsTCA (CFTR) ENSP00000514466.1:n.*34_*36delinsTCA
ENST00000699598.1:c.1476_1478delinsTCA (CFTR) ENSP00000514467.1:p.Ser492=
ENST00000699599.1:c.1476_1478delinsTCA (CFTR) ENSP00000514468.1:p.Ser492=
ENST00000699600.1:c.1476_1478delinsTCA (CFTR) ENSP00000514469.1:p.Ser492=
ENST00000699601.1:c.1476_1478delinsTCA (CFTR) ENSP00000514470.1:p.Ser492=
ENST00000699602.1:c.1476_1478delinsTCA (CFTR) ENSP00000514471.1:p.Ser492=
ENST00000699604.1:c.*1300_*1302delinsTCA (CFTR) ENSP00000514472.1:n.*1300_*1302delinsTCA
ENST00000699605.1:c.1050_1052delinsTCA (CFTR) ENSP00000514473.1:p.Ser350=
ENST00000003084.11:c.1476_1478delinsTCA (CFTR) MANE Select ENSP00000003084.6:p.Ser492=
ENST00000647978.1:c.*1190_*1192delinsTCA (CFTR) ENSP00000497658.1:n.*1190_*1192delinsTCA
ENST00000648260.1:c.1293_1295delinsTCA (CFTR) ENSP00000497957.1:p.Ser431=
ENST00000649406.1:c.1293_1295delinsTCA (CFTR) ENSP00000497965.1:p.Ser431=
ENST00000649781.1:c.1293_1295delinsTCA (CFTR) ENSP00000497203.1:p.Ser431=
ENST00000003084.10:c.1476_1478delinsTCA (CFTR) ENSP00000003084.6:p.Ser492=
ENST00000426809.5:c.1386_1388delinsTCA (CFTR) ENSP00000389119.1:p.Ser462=
NM_000492.3:c.1476_1478delinsTCA , LRG_663t1:c.1476_1478delinsTCA (CFTR) NP_000483.3:p.Ser492=
XM_011515751.1:c.1566_1568delinsTCA (CFTR) XP_011514053.1:p.Ser522=
XM_011515752.1:c.1566_1568delinsTCA (CFTR) XP_011514054.1:p.Ser522=
XM_011515753.1:c.1233_1235delinsTCA (CFTR) XP_011514055.1:p.Ser411=
XM_011515754.1:c.1233_1235delinsTCA (CFTR) XP_011514056.1:p.Ser411=
NR_149084.1:n.221+1184_221+1186delinsTGA (CFTR-AS1)
NM_000492.4:c.1476_1478delinsTCA (CFTR) MANE Select NP_000483.3:p.Ser492=