Canonical Allele Identifier: CA327302

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117642561C>T , CM000669.2:g.117642561C>T	GRCh38
NC_000007.13:g.117282615C>T , CM000669.1:g.117282615C>T	GRCh37
NC_000007.12:g.117069851C>T	NCBI36
NG_016465.4:g.181778C>T , LRG_663:g.181778C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000492.4:c.3841C>T MANE Select	NP_000483.3:p.Gln1281Ter
ENST00000003084.11:c.3841C>T MANE Select	ENSP00000003084.6:p.Gln1281Ter
NM_000492.3:c.3841C>T , LRG_663t1:c.3841C>T	NP_000483.3:p.Gln1281Ter
ENST00000003084.10:c.3841C>T	ENSP00000003084.6:p.Gln1281Ter
ENST00000426809.5:c.3751C>T	ENSP00000389119.1:p.Gln1251Ter
ENST00000647720.1:c.1291C>T
ENST00000647720.2:c.*50C>T	ENSP00000497673.2:n.*50C>T
ENST00000647978.2:c.*3555C>T	ENSP00000497658.1:n.*3555C>T
ENST00000649781.1:c.3658C>T	ENSP00000497203.1:p.Gln1220Ter
ENST00000649781.2:c.3658C>T	ENSP00000497203.1:p.Gln1220Ter
ENST00000685018.1:c.589C>T	ENSP00000510194.1:p.Gln197Ter
ENST00000685018.2:c.3841C>T	ENSP00000510194.2:p.Gln1281Ter
ENST00000687278.1:c.1628C>T	ENSP00000509593.1:n.1628C>T
ENST00000687278.2:c.*494C>T	ENSP00000509593.2:n.*494C>T
ENST00000689011.1:c.423C>T
ENST00000699585.1:c.*50C>T	ENSP00000514456.1:n.*50C>T
ENST00000699598.1:c.3841C>T	ENSP00000514467.1:p.Gln1281Ter
ENST00000699599.1:c.3841C>T	ENSP00000514468.1:p.Gln1281Ter
ENST00000699600.1:c.*502C>T	ENSP00000514469.1:n.*502C>T
ENST00000699601.1:c.*2216C>T	ENSP00000514470.1:n.*2216C>T
ENST00000699602.1:c.3835C>T	ENSP00000514471.1:p.Gln1279Ter
ENST00000699604.1:c.*3665C>T	ENSP00000514472.1:n.*3665C>T
ENST00000699605.1:c.3415C>T	ENSP00000514473.1:p.Gln1139Ter
XM_011515751.1:c.3931C>T	XP_011514053.1:p.Gln1311Ter
XM_011515752.1:c.3931C>T	XP_011514054.1:p.Gln1311Ter
XM_011515753.1:c.3598C>T	XP_011514055.1:p.Gln1200Ter
XM_011515754.1:c.3598C>T	XP_011514056.1:p.Gln1200Ter