Canonical Allele Identifier: CA368974532
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117642468A>G , CM000669.2:g.117642468A>G GRCh38
NC_000007.13:g.117282522A>G , CM000669.1:g.117282522A>G GRCh37
NC_000007.12:g.117069758A>G NCBI36
NG_016465.4:g.181685A>G , LRG_663:g.181685A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.3548A>G ENSP00000497673.2:p.Glu1183Gly
ENST00000647978.2:c.*3462A>G ENSP00000497658.1:n.*3462A>G
ENST00000649781.2:c.3565A>G ENSP00000497203.1:p.Lys1189Glu
ENST00000685018.2:c.3748A>G ENSP00000510194.2:p.Lys1250Glu
ENST00000687278.2:c.*401A>G ENSP00000509593.2:n.*401A>G
ENST00000699585.1:c.3548A>G ENSP00000514456.1:p.Glu1183Gly
ENST00000699598.1:c.3748A>G ENSP00000514467.1:p.Lys1250Glu
ENST00000699599.1:c.3748A>G ENSP00000514468.1:p.Lys1250Glu
ENST00000699600.1:c.*409A>G ENSP00000514469.1:n.*409A>G
ENST00000699601.1:c.*2123A>G ENSP00000514470.1:n.*2123A>G
ENST00000699602.1:c.3742A>G ENSP00000514471.1:p.Lys1248Glu
ENST00000699604.1:c.*3572A>G ENSP00000514472.1:n.*3572A>G
ENST00000699605.1:c.3322A>G ENSP00000514473.1:p.Lys1108Glu
ENST00000685018.1:c.496A>G ENSP00000510194.1:p.Lys166Glu
ENST00000687278.1:c.1535A>G ENSP00000509593.1:n.1535A>G
ENST00000689011.1:c.330A>G
ENST00000003084.11:c.3748A>G MANE Select ENSP00000003084.6:p.Lys1250Glu
ENST00000647720.1:c.1198A>G
ENST00000649781.1:c.3565A>G ENSP00000497203.1:p.Lys1189Glu
ENST00000003084.10:c.3748A>G ENSP00000003084.6:p.Lys1250Glu
ENST00000426809.5:c.3658A>G ENSP00000389119.1:p.Lys1220Glu
NM_000492.3:c.3748A>G , LRG_663t1:c.3748A>G NP_000483.3:p.Lys1250Glu
XM_011515751.1:c.3838A>G XP_011514053.1:p.Lys1280Glu
XM_011515752.1:c.3838A>G XP_011514054.1:p.Lys1280Glu
XM_011515753.1:c.3505A>G XP_011514055.1:p.Lys1169Glu
XM_011515754.1:c.3505A>G XP_011514056.1:p.Lys1169Glu
NM_000492.4:c.3748A>G MANE Select NP_000483.3:p.Lys1250Glu