Canonical Allele Identifier: CA368992552
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117611768C>G , CM000669.2:g.117611768C>G GRCh38
NC_000007.13:g.117251822C>G , CM000669.1:g.117251822C>G GRCh37
NC_000007.12:g.117039058C>G NCBI36
NG_016465.4:g.150985C>G , LRG_663:g.150985C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.3327C>G ENSP00000497673.2:p.Ile1109Met
ENST00000647978.2:c.*3041C>G ENSP00000497658.1:n.*3041C>G
ENST00000649781.2:c.3144C>G ENSP00000497203.1:p.Ile1048Met
ENST00000685018.2:c.3327C>G ENSP00000510194.2:p.Ile1109Met
ENST00000687278.2:c.3327C>G ENSP00000509593.2:p.Ile1109Met
ENST00000699585.1:c.3327C>G ENSP00000514456.1:p.Ile1109Met
ENST00000699598.1:c.3327C>G ENSP00000514467.1:p.Ile1109Met
ENST00000699599.1:c.3327C>G ENSP00000514468.1:p.Ile1109Met
ENST00000699600.1:c.3327C>G ENSP00000514469.1:p.Ile1109Met
ENST00000699601.1:c.*1627C>G ENSP00000514470.1:n.*1627C>G
ENST00000699602.1:c.3327C>G ENSP00000514471.1:p.Ile1109Met
ENST00000699604.1:c.*3151C>G ENSP00000514472.1:n.*3151C>G
ENST00000699605.1:c.2901C>G ENSP00000514473.1:p.Ile967Met
ENST00000685018.1:c.75C>G ENSP00000510194.1:p.Ile25Met
ENST00000687278.1:c.918C>G ENSP00000509593.1:p.Ile306Met
ENST00000003084.11:c.3327C>G MANE Select ENSP00000003084.6:p.Ile1109Met
ENST00000647720.1:c.977C>G
ENST00000648260.1:c.2109C>G ENSP00000497957.1:p.Ile703Met
ENST00000649406.1:c.3144C>G ENSP00000497965.1:p.Ile1048Met
ENST00000649781.1:c.3144C>G ENSP00000497203.1:p.Ile1048Met
ENST00000003084.10:c.3327C>G ENSP00000003084.6:p.Ile1109Met
ENST00000426809.5:c.3237C>G ENSP00000389119.1:p.Ile1079Met
ENST00000468795.1:c.152C>G
NM_000492.3:c.3327C>G , LRG_663t1:c.3327C>G NP_000483.3:p.Ile1109Met
XM_011515751.1:c.3417C>G XP_011514053.1:p.Ile1139Met
XM_011515752.1:c.3417C>G XP_011514054.1:p.Ile1139Met
XM_011515753.1:c.3084C>G XP_011514055.1:p.Ile1028Met
XM_011515754.1:c.3084C>G XP_011514056.1:p.Ile1028Met
NM_000492.4:c.3327C>G MANE Select NP_000483.3:p.Ile1109Met