Canonical Allele Identifier: CA1737374590

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603585C= , CM000669.2:g.117603585C=	GRCh38
NC_000007.13:g.117243639C= , CM000669.1:g.117243639C=	GRCh37
NC_000007.12:g.117030875C=	NCBI36
NG_016465.4:g.142802C= , LRG_663:g.142802C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2711C=	ENSP00000497673.2:p.Ala904=
ENST00000647978.2:c.*2425C=	ENSP00000497658.1:n.*2425C=
ENST00000649781.2:c.2528C=	ENSP00000497203.1:p.Ala843=
ENST00000685018.2:c.2711C=	ENSP00000510194.2:p.Ala904=
ENST00000687278.2:c.2711C=	ENSP00000509593.2:p.Ala904=
ENST00000699585.1:c.2711C=	ENSP00000514456.1:p.Ala904=
ENST00000699598.1:c.2711C=	ENSP00000514467.1:p.Ala904=
ENST00000699599.1:c.2711C=	ENSP00000514468.1:p.Ala904=
ENST00000699600.1:c.2711C=	ENSP00000514469.1:p.Ala904=
ENST00000699601.1:c.*1011C=	ENSP00000514470.1:n.*1011C=
ENST00000699602.1:c.2711C=	ENSP00000514471.1:p.Ala904=
ENST00000699604.1:c.*2535C=	ENSP00000514472.1:n.*2535C=
ENST00000699605.1:c.2285C=	ENSP00000514473.1:p.Ala762=
ENST00000687278.1:c.302C=	ENSP00000509593.1:p.Ala101=
ENST00000003084.11:c.2711C= MANE Select	ENSP00000003084.6:p.Ala904=
ENST00000647720.1:c.361C=
ENST00000648260.1:c.1493C=	ENSP00000497957.1:p.Ala498=
ENST00000649406.1:c.2528C=	ENSP00000497965.1:p.Ala843=
ENST00000649781.1:c.2528C=	ENSP00000497203.1:p.Ala843=
ENST00000003084.10:c.2711C=	ENSP00000003084.6:p.Ala904=
ENST00000426809.5:c.2621C=	ENSP00000389119.1:p.Ala874=
NM_000492.3:c.2711C= , LRG_663t1:c.2711C=	NP_000483.3:p.Ala904=
XM_011515751.1:c.2801C=	XP_011514053.1:p.Ala934=
XM_011515752.1:c.2801C=	XP_011514054.1:p.Ala934=
XM_011515753.1:c.2468C=	XP_011514055.1:p.Ala823=
XM_011515754.1:c.2468C=	XP_011514056.1:p.Ala823=
NM_000492.4:c.2711C= MANE Select	NP_000483.3:p.Ala904=