Canonical Allele Identifier: CA1737370175

Gene: CFTR CFTR-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117548760_117548764delinsTATTA , CM000669.2:g.117548760_117548764delinsTATTA	GRCh38
NC_000007.13:g.117188814_117188818delinsTATTA , CM000669.1:g.117188814_117188818delinsTATTA	GRCh37
NC_000007.12:g.116976050_116976054delinsTATTA	NCBI36
NG_016465.4:g.87977_87981delinsTATTA , LRG_663:g.87977_87981delinsTATTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.1329_1333delinsTATTA (CFTR)	ENSP00000497673.2:p.Asp443=
ENST00000647978.2:c.*1106+6652_*1106+6656delinsTATTA (CFTR)	ENSP00000497658.1:n.*1106+6652_*1106+6656delinsTATTA
ENST00000649781.2:c.1209+6652_1209+6656delinsTATTA (CFTR)	ENSP00000497203.1:n.1209+6652_1209+6656delinsTATTA
ENST00000685018.2:c.1329_1333delinsTATTA (CFTR)	ENSP00000510194.2:p.Asp443=
ENST00000687278.2:c.1329_1333delinsTATTA (CFTR)	ENSP00000509593.2:p.Asp443=
ENST00000699585.1:c.1329_1333delinsTATTA (CFTR)	ENSP00000514456.1:p.Asp443=
ENST00000699596.1:c.1329_1333delinsTATTA (CFTR)	ENSP00000514465.1:p.Asp443=
ENST00000699597.1:c.1329_1333delinsTATTA (CFTR)	ENSP00000514466.1:p.Asp443=
ENST00000699598.1:c.1329_1333delinsTATTA (CFTR)	ENSP00000514467.1:p.Asp443=
ENST00000699599.1:c.1329_1333delinsTATTA (CFTR)	ENSP00000514468.1:p.Asp443=
ENST00000699600.1:c.1329_1333delinsTATTA (CFTR)	ENSP00000514469.1:p.Asp443=
ENST00000699601.1:c.1329_1333delinsTATTA (CFTR)	ENSP00000514470.1:p.Asp443=
ENST00000699602.1:c.1329_1333delinsTATTA (CFTR)	ENSP00000514471.1:p.Asp443=
ENST00000699604.1:c.*1153_*1157delinsTATTA (CFTR)	ENSP00000514472.1:n.*1153_*1157delinsTATTA
ENST00000699605.1:c.966+6652_966+6656delinsTATTA (CFTR)	ENSP00000514473.1:n.966+6652_966+6656delinsTATTA
ENST00000003084.11:c.1329_1333delinsTATTA (CFTR) MANE Select	ENSP00000003084.6:p.Asp443=
ENST00000647978.1:c.*1106+6652_*1106+6656delinsTATTA (CFTR)	ENSP00000497658.1:n.*1106+6652_*1106+6656delinsTATTA
ENST00000648260.1:c.1209+6652_1209+6656delinsTATTA (CFTR)	ENSP00000497957.1:n.1209+6652_1209+6656delinsTATTA
ENST00000649406.1:c.1209+6652_1209+6656delinsTATTA (CFTR)	ENSP00000497965.1:n.1209+6652_1209+6656delinsTATTA
ENST00000649781.1:c.1209+6652_1209+6656delinsTATTA (CFTR)	ENSP00000497203.1:n.1209+6652_1209+6656delinsTATTA
ENST00000003084.10:c.1329_1333delinsTATTA (CFTR)	ENSP00000003084.6:p.Asp443=
ENST00000426809.5:c.1239_1243delinsTATTA (CFTR)	ENSP00000389119.1:p.Asp413=
NM_000492.3:c.1329_1333delinsTATTA , LRG_663t1:c.1329_1333delinsTATTA (CFTR)	NP_000483.3:p.Asp443=
XM_011515751.1:c.1419_1423delinsTATTA (CFTR)	XP_011514053.1:p.Asp473=
XM_011515752.1:c.1419_1423delinsTATTA (CFTR)	XP_011514054.1:p.Asp473=
XM_011515753.1:c.1086_1090delinsTATTA (CFTR)	XP_011514055.1:p.Asp362=
XM_011515754.1:c.1086_1090delinsTATTA (CFTR)	XP_011514056.1:p.Asp362=
NR_149084.1:n.222-6225_222-6221delinsTAATA (CFTR-AS1)
NM_000492.4:c.1329_1333delinsTATTA (CFTR) MANE Select	NP_000483.3:p.Asp443=