Canonical Allele Identifier: CA2695208419
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117603653_117603662dup , CM000669.2:g.117603653_117603662dup GRCh38
NC_000007.13:g.117243707_117243716dup , CM000669.1:g.117243707_117243716dup GRCh37
NC_000007.12:g.117030943_117030952dup NCBI36
NG_016465.4:g.142870_142879dup , LRG_663:g.142870_142879dup

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.2779_2788dup ENSP00000497673.2:p.Gly930AlafsTer?
ENST00000647978.2:c.*2493_*2502dup ENSP00000497658.1:n.*2493_*2502dup
ENST00000649781.2:c.2596_2605dup ENSP00000497203.1:p.Gly869AlafsTer?
ENST00000685018.2:c.2779_2788dup ENSP00000510194.2:p.Gly930AlafsTer?
ENST00000687278.2:c.2779_2788dup ENSP00000509593.2:p.Gly930AlafsTer?
ENST00000699585.1:c.2779_2788dup ENSP00000514456.1:p.Gly930AlafsTer?
ENST00000699598.1:c.2779_2788dup ENSP00000514467.1:p.Gly930AlafsTer?
ENST00000699599.1:c.2779_2788dup ENSP00000514468.1:p.Gly930AlafsTer?
ENST00000699600.1:c.2779_2788dup ENSP00000514469.1:p.Gly930AlafsTer?
ENST00000699601.1:c.*1079_*1088dup ENSP00000514470.1:n.*1079_*1088dup
ENST00000699602.1:c.2779_2788dup ENSP00000514471.1:p.Gly930AlafsTer?
ENST00000699604.1:c.*2603_*2612dup ENSP00000514472.1:n.*2603_*2612dup
ENST00000699605.1:c.2353_2362dup ENSP00000514473.1:p.Gly788AlafsTer?
ENST00000687278.1:c.370_379dup ENSP00000509593.1:p.Gly127AlafsTer?
ENST00000003084.11:c.2779_2788dup MANE Select ENSP00000003084.6:p.Gly930AlafsTer?
ENST00000647720.1:c.429_438dup
ENST00000648260.1:c.1561_1570dup ENSP00000497957.1:p.Gly524AlafsTer?
ENST00000649406.1:c.2596_2605dup ENSP00000497965.1:p.Gly869AlafsTer?
ENST00000649781.1:c.2596_2605dup ENSP00000497203.1:p.Gly869AlafsTer?
ENST00000003084.10:c.2779_2788dup ENSP00000003084.6:p.Gly930AlafsTer?
ENST00000426809.5:c.2689_2698dup ENSP00000389119.1:p.Gly900AlafsTer?
NM_000492.3:c.2779_2788dup , LRG_663t1:c.2779_2788dup NP_000483.3:p.Gly930AlafsTer?
XM_011515751.1:c.2869_2878dup XP_011514053.1:p.Gly960AlafsTer?
XM_011515752.1:c.2869_2878dup XP_011514054.1:p.Gly960AlafsTer?
XM_011515753.1:c.2536_2545dup XP_011514055.1:p.Gly849AlafsTer?
XM_011515754.1:c.2536_2545dup XP_011514056.1:p.Gly849AlafsTer?
NM_000492.4:c.2779_2788dup MANE Select NP_000483.3:p.Gly930AlafsTer?