Canonical Allele Identifier: CA368993491

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117254714A>T (hg19) ; chr7:g.117614660A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117614660A>T , CM000669.2:g.117614660A>T	GRCh38
NC_000007.13:g.117254714A>T , CM000669.1:g.117254714A>T	GRCh37
NC_000007.12:g.117041950A>T	NCBI36
NG_016465.4:g.153877A>T , LRG_663:g.153877A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3415A>T	ENSP00000497673.2:p.Ile1139Phe
ENST00000647978.2:c.*3129A>T	ENSP00000497658.1:n.*3129A>T
ENST00000649781.2:c.3232A>T	ENSP00000497203.1:p.Ile1078Phe
ENST00000685018.2:c.3415A>T	ENSP00000510194.2:p.Ile1139Phe
ENST00000687278.2:c.3415A>T	ENSP00000509593.2:p.Ile1139Phe
ENST00000699585.1:c.3415A>T	ENSP00000514456.1:p.Ile1139Phe
ENST00000699598.1:c.3415A>T	ENSP00000514467.1:p.Ile1139Phe
ENST00000699599.1:c.3415A>T	ENSP00000514468.1:p.Ile1139Phe
ENST00000699600.1:c.3415A>T	ENSP00000514469.1:p.Ile1139Phe
ENST00000699601.1:c.*1790A>T	ENSP00000514470.1:n.*1790A>T
ENST00000699602.1:c.3409A>T	ENSP00000514471.1:p.Ile1137Phe
ENST00000699604.1:c.*3239A>T	ENSP00000514472.1:n.*3239A>T
ENST00000699605.1:c.2989A>T	ENSP00000514473.1:p.Ile997Phe
ENST00000685018.1:c.163A>T	ENSP00000510194.1:p.Ile55Phe
ENST00000687278.1:c.1006A>T	ENSP00000509593.1:p.Ile336Phe
ENST00000003084.11:c.3415A>T MANE Select	ENSP00000003084.6:p.Ile1139Phe
ENST00000647720.1:c.1065A>T
ENST00000648260.1:c.2197A>T	ENSP00000497957.1:p.Ile733Phe
ENST00000649406.1:c.3232A>T	ENSP00000497965.1:p.Ile1078Phe
ENST00000649781.1:c.3232A>T	ENSP00000497203.1:p.Ile1078Phe
ENST00000003084.10:c.3415A>T	ENSP00000003084.6:p.Ile1139Phe
ENST00000426809.5:c.3325A>T	ENSP00000389119.1:p.Ile1109Phe
ENST00000468795.1:c.240A>T
NM_000492.3:c.3415A>T , LRG_663t1:c.3415A>T	NP_000483.3:p.Ile1139Phe
XM_011515751.1:c.3505A>T	XP_011514053.1:p.Ile1169Phe
XM_011515752.1:c.3505A>T	XP_011514054.1:p.Ile1169Phe
XM_011515753.1:c.3172A>T	XP_011514055.1:p.Ile1058Phe
XM_011515754.1:c.3172A>T	XP_011514056.1:p.Ile1058Phe
NM_000492.4:c.3415A>T MANE Select	NP_000483.3:p.Ile1139Phe