Canonical Allele Identifier: CA368997115
Gene: CFTR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117627652A>T , CM000669.2:g.117627652A>T GRCh38
NC_000007.13:g.117267706A>T , CM000669.1:g.117267706A>T GRCh37
NC_000007.12:g.117054942A>T NCBI36
NG_016465.4:g.166869A>T , LRG_663:g.166869A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.3517+82A>T ENSP00000497673.2:n.3517+82A>T
ENST00000647978.2:c.*3313A>T ENSP00000497658.1:n.*3313A>T
ENST00000649781.2:c.3416A>T ENSP00000497203.1:p.Lys1139Ile
ENST00000685018.2:c.3599A>T ENSP00000510194.2:p.Lys1200Ile
ENST00000687278.2:c.*252A>T ENSP00000509593.2:n.*252A>T
ENST00000699585.1:c.3517+82A>T ENSP00000514456.1:n.3517+82A>T
ENST00000699598.1:c.3599A>T ENSP00000514467.1:p.Lys1200Ile
ENST00000699599.1:c.3599A>T ENSP00000514468.1:p.Lys1200Ile
ENST00000699600.1:c.*260A>T ENSP00000514469.1:n.*260A>T
ENST00000699601.1:c.*1974A>T ENSP00000514470.1:n.*1974A>T
ENST00000699602.1:c.3593A>T ENSP00000514471.1:p.Lys1198Ile
ENST00000699604.1:c.*3423A>T ENSP00000514472.1:n.*3423A>T
ENST00000699605.1:c.3173A>T ENSP00000514473.1:p.Lys1058Ile
ENST00000685018.1:c.347A>T ENSP00000510194.1:p.Lys116Ile
ENST00000687278.1:c.1386A>T ENSP00000509593.1:n.1386A>T
ENST00000689011.1:c.181A>T
ENST00000003084.11:c.3599A>T MANE Select ENSP00000003084.6:p.Lys1200Ile
ENST00000647720.1:c.1167+82A>T
ENST00000648260.1:c.2381A>T ENSP00000497957.1:p.Lys794Ile
ENST00000649406.1:c.3416A>T ENSP00000497965.1:p.Lys1139Ile
ENST00000649781.1:c.3416A>T ENSP00000497203.1:p.Lys1139Ile
ENST00000003084.10:c.3599A>T ENSP00000003084.6:p.Lys1200Ile
ENST00000426809.5:c.3509A>T ENSP00000389119.1:p.Lys1170Ile
ENST00000468795.1:c.424A>T
NM_000492.3:c.3599A>T , LRG_663t1:c.3599A>T NP_000483.3:p.Lys1200Ile
XM_011515751.1:c.3689A>T XP_011514053.1:p.Lys1230Ile
XM_011515752.1:c.3689A>T XP_011514054.1:p.Lys1230Ile
XM_011515753.1:c.3356A>T XP_011514055.1:p.Lys1119Ile
XM_011515754.1:c.3356A>T XP_011514056.1:p.Lys1119Ile
NM_000492.4:c.3599A>T MANE Select NP_000483.3:p.Lys1200Ile