Canonical Allele Identifier: CA1737375457

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603748_117603749delinsAG , CM000669.2:g.117603748_117603749delinsAG	GRCh38
NC_000007.13:g.117243802_117243803delinsAG , CM000669.1:g.117243802_117243803delinsAG	GRCh37
NC_000007.12:g.117031038_117031039delinsAG	NCBI36
NG_016465.4:g.142965_142966delinsAG , LRG_663:g.142965_142966delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.2874_2875delinsAG	ENSP00000497673.2:p.Gln958=
ENST00000647978.2:c.*2588_*2589delinsAG	ENSP00000497658.1:n.*2588_*2589delinsAG
ENST00000649781.2:c.2691_2692delinsAG	ENSP00000497203.1:p.Gln897=
ENST00000685018.2:c.2874_2875delinsAG	ENSP00000510194.2:p.Gln958=
ENST00000687278.2:c.2874_2875delinsAG	ENSP00000509593.2:p.Gln958=
ENST00000699585.1:c.2874_2875delinsAG	ENSP00000514456.1:p.Gln958=
ENST00000699598.1:c.2874_2875delinsAG	ENSP00000514467.1:p.Gln958=
ENST00000699599.1:c.2874_2875delinsAG	ENSP00000514468.1:p.Gln958=
ENST00000699600.1:c.2874_2875delinsAG	ENSP00000514469.1:p.Gln958=
ENST00000699601.1:c.*1174_*1175delinsAG	ENSP00000514470.1:n.*1174_*1175delinsAG
ENST00000699602.1:c.2874_2875delinsAG	ENSP00000514471.1:p.Gln958=
ENST00000699604.1:c.*2698_*2699delinsAG	ENSP00000514472.1:n.*2698_*2699delinsAG
ENST00000699605.1:c.2448_2449delinsAG	ENSP00000514473.1:p.Gln816=
ENST00000687278.1:c.465_466delinsAG	ENSP00000509593.1:p.Gln155=
ENST00000003084.11:c.2874_2875delinsAG MANE Select	ENSP00000003084.6:p.Gln958=
ENST00000647720.1:c.524_525delinsAG
ENST00000648260.1:c.1656_1657delinsAG	ENSP00000497957.1:p.Gln552=
ENST00000649406.1:c.2691_2692delinsAG	ENSP00000497965.1:p.Gln897=
ENST00000649781.1:c.2691_2692delinsAG	ENSP00000497203.1:p.Gln897=
ENST00000003084.10:c.2874_2875delinsAG	ENSP00000003084.6:p.Gln958=
ENST00000426809.5:c.2784_2785delinsAG	ENSP00000389119.1:p.Gln928=
NM_000492.3:c.2874_2875delinsAG , LRG_663t1:c.2874_2875delinsAG	NP_000483.3:p.Gln958=
XM_011515751.1:c.2964_2965delinsAG	XP_011514053.1:p.Gln988=
XM_011515752.1:c.2964_2965delinsAG	XP_011514054.1:p.Gln988=
XM_011515753.1:c.2631_2632delinsAG	XP_011514055.1:p.Gln877=
XM_011515754.1:c.2631_2632delinsAG	XP_011514056.1:p.Gln877=
NM_000492.4:c.2874_2875delinsAG MANE Select	NP_000483.3:p.Gln958=