Canonical Allele Identifier: CA368974852

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117282559A>T (hg19) ; chr7:g.117642505A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117642505A>T , CM000669.2:g.117642505A>T	GRCh38
NC_000007.13:g.117282559A>T , CM000669.1:g.117282559A>T	GRCh37
NC_000007.12:g.117069795A>T	NCBI36
NG_016465.4:g.181722A>T , LRG_663:g.181722A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3585A>T	ENSP00000497673.2:p.Glu1195Asp
ENST00000647978.2:c.*3499A>T	ENSP00000497658.1:n.*3499A>T
ENST00000649781.2:c.3602A>T	ENSP00000497203.1:p.Asn1201Ile
ENST00000685018.2:c.3785A>T	ENSP00000510194.2:p.Asn1262Ile
ENST00000687278.2:c.*438A>T	ENSP00000509593.2:n.*438A>T
ENST00000699585.1:c.3585A>T	ENSP00000514456.1:p.Glu1195Asp
ENST00000699598.1:c.3785A>T	ENSP00000514467.1:p.Asn1262Ile
ENST00000699599.1:c.3785A>T	ENSP00000514468.1:p.Asn1262Ile
ENST00000699600.1:c.*446A>T	ENSP00000514469.1:n.*446A>T
ENST00000699601.1:c.*2160A>T	ENSP00000514470.1:n.*2160A>T
ENST00000699602.1:c.3779A>T	ENSP00000514471.1:p.Asn1260Ile
ENST00000699604.1:c.*3609A>T	ENSP00000514472.1:n.*3609A>T
ENST00000699605.1:c.3359A>T	ENSP00000514473.1:p.Asn1120Ile
ENST00000685018.1:c.533A>T	ENSP00000510194.1:p.Asn178Ile
ENST00000687278.1:c.1572A>T	ENSP00000509593.1:n.1572A>T
ENST00000689011.1:c.367A>T
ENST00000003084.11:c.3785A>T MANE Select	ENSP00000003084.6:p.Asn1262Ile
ENST00000647720.1:c.1235A>T
ENST00000649781.1:c.3602A>T	ENSP00000497203.1:p.Asn1201Ile
ENST00000003084.10:c.3785A>T	ENSP00000003084.6:p.Asn1262Ile
ENST00000426809.5:c.3695A>T	ENSP00000389119.1:p.Asn1232Ile
NM_000492.3:c.3785A>T , LRG_663t1:c.3785A>T	NP_000483.3:p.Asn1262Ile
XM_011515751.1:c.3875A>T	XP_011514053.1:p.Asn1292Ile
XM_011515752.1:c.3875A>T	XP_011514054.1:p.Asn1292Ile
XM_011515753.1:c.3542A>T	XP_011514055.1:p.Asn1181Ile
XM_011515754.1:c.3542A>T	XP_011514056.1:p.Asn1181Ile
NM_000492.4:c.3785A>T MANE Select	NP_000483.3:p.Asn1262Ile