Canonical Allele Identifier: CA1737385431

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117610707_117610708delinsAG , CM000669.2:g.117610707_117610708delinsAG	GRCh38
NC_000007.13:g.117250761_117250762delinsAG , CM000669.1:g.117250761_117250762delinsAG	GRCh37
NC_000007.12:g.117037997_117037998delinsAG	NCBI36
NG_016465.4:g.149924_149925delinsAG , LRG_663:g.149924_149925delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3139+38_3139+39delinsAG	ENSP00000497673.2:n.3139+38_3139+39delinsAG
ENST00000647978.2:c.*2853+38_*2853+39delinsAG	ENSP00000497658.1:n.*2853+38_*2853+39delinsAG
ENST00000649781.2:c.2956+38_2956+39delinsAG	ENSP00000497203.1:n.2956+38_2956+39delinsAG
ENST00000685018.2:c.3139+38_3139+39delinsAG	ENSP00000510194.2:n.3139+38_3139+39delinsAG
ENST00000687278.2:c.3139+38_3139+39delinsAG	ENSP00000509593.2:n.3139+38_3139+39delinsAG
ENST00000699585.1:c.3139+38_3139+39delinsAG	ENSP00000514456.1:n.3139+38_3139+39delinsAG
ENST00000699598.1:c.3139+38_3139+39delinsAG	ENSP00000514467.1:n.3139+38_3139+39delinsAG
ENST00000699599.1:c.3139+38_3139+39delinsAG	ENSP00000514468.1:n.3139+38_3139+39delinsAG
ENST00000699600.1:c.3139+38_3139+39delinsAG	ENSP00000514469.1:n.3139+38_3139+39delinsAG
ENST00000699601.1:c.*1439+38_*1439+39delinsAG	ENSP00000514470.1:n.*1439+38_*1439+39delinsAG
ENST00000699602.1:c.3139+38_3139+39delinsAG	ENSP00000514471.1:n.3139+38_3139+39delinsAG
ENST00000699604.1:c.*2963+38_*2963+39delinsAG	ENSP00000514472.1:n.*2963+38_*2963+39delinsAG
ENST00000699605.1:c.2713+38_2713+39delinsAG	ENSP00000514473.1:n.2713+38_2713+39delinsAG
ENST00000687278.1:c.730+38_730+39delinsAG	ENSP00000509593.1:n.730+38_730+39delinsAG
ENST00000003084.11:c.3139+38_3139+39delinsAG MANE Select	ENSP00000003084.6:n.3139+38_3139+39delinsAG
ENST00000647720.1:c.789+38_789+39delinsAG
ENST00000648260.1:c.1921+38_1921+39delinsAG	ENSP00000497957.1:n.1921+38_1921+39delinsAG
ENST00000649406.1:c.2956+38_2956+39delinsAG	ENSP00000497965.1:n.2956+38_2956+39delinsAG
ENST00000649781.1:c.2956+38_2956+39delinsAG	ENSP00000497203.1:n.2956+38_2956+39delinsAG
ENST00000003084.10:c.3139+38_3139+39delinsAG	ENSP00000003084.6:n.3139+38_3139+39delinsAG
ENST00000426809.5:c.3049+38_3049+39delinsAG	ENSP00000389119.1:n.3049+38_3049+39delinsAG
NM_000492.3:c.3139+38_3139+39delinsAG , LRG_663t1:c.3139+38_3139+39delinsAG	NP_000483.3:n.3139+38_3139+39delinsAG
XM_011515751.1:c.3229+38_3229+39delinsAG	XP_011514053.1:n.3229+38_3229+39delinsAG
XM_011515752.1:c.3229+38_3229+39delinsAG	XP_011514054.1:n.3229+38_3229+39delinsAG
XM_011515753.1:c.2896+38_2896+39delinsAG	XP_011514055.1:n.2896+38_2896+39delinsAG
XM_011515754.1:c.2896+38_2896+39delinsAG	XP_011514056.1:n.2896+38_2896+39delinsAG
NM_000492.4:c.3139+38_3139+39delinsAG MANE Select	NP_000483.3:n.3139+38_3139+39delinsAG