Canonical Allele Identifier: CA1737387116
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117611679A= , CM000669.2:g.117611679A= GRCh38
NC_000007.13:g.117251733A= , CM000669.1:g.117251733A= GRCh37
NC_000007.12:g.117038969A= NCBI36
NG_016465.4:g.150896A= , LRG_663:g.150896A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.3238A= ENSP00000497673.2:p.Lys1080=
ENST00000647978.2:c.*2952A= ENSP00000497658.1:n.*2952A=
ENST00000649781.2:c.3055A= ENSP00000497203.1:p.Lys1019=
ENST00000685018.2:c.3238A= ENSP00000510194.2:p.Lys1080=
ENST00000687278.2:c.3238A= ENSP00000509593.2:p.Lys1080=
ENST00000699585.1:c.3238A= ENSP00000514456.1:p.Lys1080=
ENST00000699598.1:c.3238A= ENSP00000514467.1:p.Lys1080=
ENST00000699599.1:c.3238A= ENSP00000514468.1:p.Lys1080=
ENST00000699600.1:c.3238A= ENSP00000514469.1:p.Lys1080=
ENST00000699601.1:c.*1538A= ENSP00000514470.1:n.*1538A=
ENST00000699602.1:c.3238A= ENSP00000514471.1:p.Lys1080=
ENST00000699604.1:c.*3062A= ENSP00000514472.1:n.*3062A=
ENST00000699605.1:c.2812A= ENSP00000514473.1:p.Lys938=
ENST00000687278.1:c.829A= ENSP00000509593.1:p.Lys277=
ENST00000003084.11:c.3238A= MANE Select ENSP00000003084.6:p.Lys1080=
ENST00000647720.1:c.888A=
ENST00000648260.1:c.2020A= ENSP00000497957.1:p.Lys674=
ENST00000649406.1:c.3055A= ENSP00000497965.1:p.Lys1019=
ENST00000649781.1:c.3055A= ENSP00000497203.1:p.Lys1019=
ENST00000003084.10:c.3238A= ENSP00000003084.6:p.Lys1080=
ENST00000426809.5:c.3148A= ENSP00000389119.1:p.Lys1050=
ENST00000468795.1:c.63A=
NM_000492.3:c.3238A= , LRG_663t1:c.3238A= NP_000483.3:p.Lys1080=
XM_011515751.1:c.3328A= XP_011514053.1:p.Lys1110=
XM_011515752.1:c.3328A= XP_011514054.1:p.Lys1110=
XM_011515753.1:c.2995A= XP_011514055.1:p.Lys999=
XM_011515754.1:c.2995A= XP_011514056.1:p.Lys999=
NM_000492.4:c.3238A= MANE Select NP_000483.3:p.Lys1080=