Canonical Allele Identifier: CA1737332753

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117540344_117540345delinsCA , CM000669.2:g.117540344_117540345delinsCA	GRCh38
NC_000007.13:g.117180398_117180399delinsCA , CM000669.1:g.117180398_117180399delinsCA	GRCh37
NC_000007.12:g.116967634_116967635delinsCA	NCBI36
NG_016465.4:g.79561_79562delinsCA , LRG_663:g.79561_79562delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.1114_1115delinsCA	ENSP00000497673.2:p.Gln372=
ENST00000647978.2:c.*1011_*1012delinsCA	ENSP00000497658.1:n.*1011_*1012delinsCA
ENST00000649781.2:c.1114_1115delinsCA	ENSP00000497203.1:p.Gln372=
ENST00000685018.2:c.1114_1115delinsCA	ENSP00000510194.2:p.Gln372=
ENST00000687278.2:c.1114_1115delinsCA	ENSP00000509593.2:p.Gln372=
ENST00000699585.1:c.1114_1115delinsCA	ENSP00000514456.1:p.Gln372=
ENST00000699596.1:c.1114_1115delinsCA	ENSP00000514465.1:p.Gln372=
ENST00000699597.1:c.1114_1115delinsCA	ENSP00000514466.1:p.Gln372=
ENST00000699598.1:c.1114_1115delinsCA	ENSP00000514467.1:p.Gln372=
ENST00000699599.1:c.1114_1115delinsCA	ENSP00000514468.1:p.Gln372=
ENST00000699600.1:c.1114_1115delinsCA	ENSP00000514469.1:p.Gln372=
ENST00000699601.1:c.1114_1115delinsCA	ENSP00000514470.1:p.Gln372=
ENST00000699602.1:c.1114_1115delinsCA	ENSP00000514471.1:p.Gln372=
ENST00000699604.1:c.*938_*939delinsCA	ENSP00000514472.1:n.*938_*939delinsCA
ENST00000699605.1:c.871_872delinsCA	ENSP00000514473.1:p.Gln291=
ENST00000003084.11:c.1114_1115delinsCA MANE Select	ENSP00000003084.6:p.Gln372=
ENST00000647978.1:c.*1011_*1012delinsCA	ENSP00000497658.1:n.*1011_*1012delinsCA
ENST00000648260.1:c.1114_1115delinsCA	ENSP00000497957.1:p.Gln372=
ENST00000649406.1:c.1114_1115delinsCA	ENSP00000497965.1:p.Gln372=
ENST00000649781.1:c.1114_1115delinsCA	ENSP00000497203.1:p.Gln372=
ENST00000673785.1:c.871_872delinsCA	ENSP00000501235.1:p.Gln291=
ENST00000003084.10:c.1114_1115delinsCA	ENSP00000003084.6:p.Gln372=
ENST00000426809.5:c.1024_1025delinsCA	ENSP00000389119.1:p.Gln342=
NM_000492.3:c.1114_1115delinsCA , LRG_663t1:c.1114_1115delinsCA	NP_000483.3:p.Gln372=
XM_011515751.1:c.1204_1205delinsCA	XP_011514053.1:p.Gln402=
XM_011515752.1:c.1204_1205delinsCA	XP_011514054.1:p.Gln402=
XM_011515753.1:c.871_872delinsCA	XP_011514055.1:p.Gln291=
XM_011515754.1:c.871_872delinsCA	XP_011514056.1:p.Gln291=
NM_000492.4:c.1114_1115delinsCA MANE Select	NP_000483.3:p.Gln372=