Canonical Allele Identifier: CA1737361719

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117534315_117534316delinsAT , CM000669.2:g.117534315_117534316delinsAT	GRCh38
NC_000007.13:g.117174369_117174370delinsAT , CM000669.1:g.117174369_117174370delinsAT	GRCh37
NC_000007.12:g.116961605_116961606delinsAT	NCBI36
NG_016465.4:g.73532_73533delinsAT , LRG_663:g.73532_73533delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.529_530delinsAT	ENSP00000497673.2:p.Ile177=
ENST00000647978.2:c.*426_*427delinsAT	ENSP00000497658.1:n.*426_*427delinsAT
ENST00000649781.2:c.529_530delinsAT	ENSP00000497203.1:p.Ile177=
ENST00000685018.2:c.529_530delinsAT	ENSP00000510194.2:p.Ile177=
ENST00000687278.2:c.529_530delinsAT	ENSP00000509593.2:p.Ile177=
ENST00000699585.1:c.529_530delinsAT	ENSP00000514456.1:p.Ile177=
ENST00000699596.1:c.529_530delinsAT	ENSP00000514465.1:p.Ile177=
ENST00000699597.1:c.529_530delinsAT	ENSP00000514466.1:p.Ile177=
ENST00000699598.1:c.529_530delinsAT	ENSP00000514467.1:p.Ile177=
ENST00000699599.1:c.529_530delinsAT	ENSP00000514468.1:p.Ile177=
ENST00000699600.1:c.529_530delinsAT	ENSP00000514469.1:p.Ile177=
ENST00000699601.1:c.529_530delinsAT	ENSP00000514470.1:p.Ile177=
ENST00000699602.1:c.529_530delinsAT	ENSP00000514471.1:p.Ile177=
ENST00000699604.1:c.*353_*354delinsAT	ENSP00000514472.1:n.*353_*354delinsAT
ENST00000699605.1:c.286_287delinsAT	ENSP00000514473.1:p.Ile96=
ENST00000003084.11:c.529_530delinsAT MANE Select	ENSP00000003084.6:p.Ile177=
ENST00000647978.1:c.*426_*427delinsAT	ENSP00000497658.1:n.*426_*427delinsAT
ENST00000648260.1:c.529_530delinsAT	ENSP00000497957.1:p.Ile177=
ENST00000649406.1:c.529_530delinsAT	ENSP00000497965.1:p.Ile177=
ENST00000649781.1:c.529_530delinsAT	ENSP00000497203.1:p.Ile177=
ENST00000673785.1:c.286_287delinsAT	ENSP00000501235.1:p.Ile96=
ENST00000003084.10:c.529_530delinsAT	ENSP00000003084.6:p.Ile177=
ENST00000426809.5:c.490-933_490-932delinsAT	ENSP00000389119.1:n.490-933_490-932delinsAT
NM_000492.3:c.529_530delinsAT , LRG_663t1:c.529_530delinsAT	NP_000483.3:p.Ile177=
XM_011515751.1:c.619_620delinsAT	XP_011514053.1:p.Ile207=
XM_011515752.1:c.619_620delinsAT	XP_011514054.1:p.Ile207=
XM_011515753.1:c.286_287delinsAT	XP_011514055.1:p.Ile96=
XM_011515754.1:c.286_287delinsAT	XP_011514056.1:p.Ile96=
NM_000492.4:c.529_530delinsAT MANE Select	NP_000483.3:p.Ile177=