Canonical Allele Identifier: CA1737386885
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117611632C= , CM000669.2:g.117611632C= GRCh38
NC_000007.13:g.117251686C= , CM000669.1:g.117251686C= GRCh37
NC_000007.12:g.117038922C= NCBI36
NG_016465.4:g.150849C= , LRG_663:g.150849C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647720.2:c.3191C= ENSP00000497673.2:p.Thr1064=
ENST00000647978.2:c.*2905C= ENSP00000497658.1:n.*2905C=
ENST00000649781.2:c.3008C= ENSP00000497203.1:p.Thr1003=
ENST00000685018.2:c.3191C= ENSP00000510194.2:p.Thr1064=
ENST00000687278.2:c.3191C= ENSP00000509593.2:p.Thr1064=
ENST00000699585.1:c.3191C= ENSP00000514456.1:p.Thr1064=
ENST00000699598.1:c.3191C= ENSP00000514467.1:p.Thr1064=
ENST00000699599.1:c.3191C= ENSP00000514468.1:p.Thr1064=
ENST00000699600.1:c.3191C= ENSP00000514469.1:p.Thr1064=
ENST00000699601.1:c.*1491C= ENSP00000514470.1:n.*1491C=
ENST00000699602.1:c.3191C= ENSP00000514471.1:p.Thr1064=
ENST00000699604.1:c.*3015C= ENSP00000514472.1:n.*3015C=
ENST00000699605.1:c.2765C= ENSP00000514473.1:p.Thr922=
ENST00000687278.1:c.782C= ENSP00000509593.1:p.Thr261=
ENST00000003084.11:c.3191C= MANE Select ENSP00000003084.6:p.Thr1064=
ENST00000647720.1:c.841C=
ENST00000648260.1:c.1973C= ENSP00000497957.1:p.Thr658=
ENST00000649406.1:c.3008C= ENSP00000497965.1:p.Thr1003=
ENST00000649781.1:c.3008C= ENSP00000497203.1:p.Thr1003=
ENST00000003084.10:c.3191C= ENSP00000003084.6:p.Thr1064=
ENST00000426809.5:c.3101C= ENSP00000389119.1:p.Thr1034=
ENST00000468795.1:c.16C=
NM_000492.3:c.3191C= , LRG_663t1:c.3191C= NP_000483.3:p.Thr1064=
XM_011515751.1:c.3281C= XP_011514053.1:p.Thr1094=
XM_011515752.1:c.3281C= XP_011514054.1:p.Thr1094=
XM_011515753.1:c.2948C= XP_011514055.1:p.Thr983=
XM_011515754.1:c.2948C= XP_011514056.1:p.Thr983=
NM_000492.4:c.3191C= MANE Select NP_000483.3:p.Thr1064=