Canonical Allele Identifier: CA1737379469

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117606683T= , CM000669.2:g.117606683T=	GRCh38
NC_000007.13:g.117246737T= , CM000669.1:g.117246737T=	GRCh37
NC_000007.12:g.117033973T=	NCBI36
NG_016465.4:g.145900T= , LRG_663:g.145900T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2918T=	ENSP00000497673.2:p.Leu973=
ENST00000647978.2:c.*2632T=	ENSP00000497658.1:n.*2632T=
ENST00000649781.2:c.2735T=	ENSP00000497203.1:p.Leu912=
ENST00000685018.2:c.2918T=	ENSP00000510194.2:p.Leu973=
ENST00000687278.2:c.2918T=	ENSP00000509593.2:p.Leu973=
ENST00000699585.1:c.2918T=	ENSP00000514456.1:p.Leu973=
ENST00000699598.1:c.2918T=	ENSP00000514467.1:p.Leu973=
ENST00000699599.1:c.2918T=	ENSP00000514468.1:p.Leu973=
ENST00000699600.1:c.2918T=	ENSP00000514469.1:p.Leu973=
ENST00000699601.1:c.*1218T=	ENSP00000514470.1:n.*1218T=
ENST00000699602.1:c.2918T=	ENSP00000514471.1:p.Leu973=
ENST00000699604.1:c.*2742T=	ENSP00000514472.1:n.*2742T=
ENST00000699605.1:c.2492T=	ENSP00000514473.1:p.Leu831=
ENST00000687278.1:c.509T=	ENSP00000509593.1:p.Leu170=
ENST00000003084.11:c.2918T= MANE Select	ENSP00000003084.6:p.Leu973=
ENST00000647720.1:c.568T=
ENST00000648260.1:c.1700T=	ENSP00000497957.1:p.Leu567=
ENST00000649406.1:c.2735T=	ENSP00000497965.1:p.Leu912=
ENST00000649781.1:c.2735T=	ENSP00000497203.1:p.Leu912=
ENST00000003084.10:c.2918T=	ENSP00000003084.6:p.Leu973=
ENST00000426809.5:c.2828T=	ENSP00000389119.1:p.Leu943=
NM_000492.3:c.2918T= , LRG_663t1:c.2918T=	NP_000483.3:p.Leu973=
XM_011515751.1:c.3008T=	XP_011514053.1:p.Leu1003=
XM_011515752.1:c.3008T=	XP_011514054.1:p.Leu1003=
XM_011515753.1:c.2675T=	XP_011514055.1:p.Leu892=
XM_011515754.1:c.2675T=	XP_011514056.1:p.Leu892=
NM_000492.4:c.2918T= MANE Select	NP_000483.3:p.Leu973=