Canonical Allele Identifier: CA1737384906

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117610571A= , CM000669.2:g.117610571A=	GRCh38
NC_000007.13:g.117250625A= , CM000669.1:g.117250625A=	GRCh37
NC_000007.12:g.117037861A=	NCBI36
NG_016465.4:g.149788A= , LRG_663:g.149788A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3041A=	ENSP00000497673.2:p.Tyr1014=
ENST00000647978.2:c.*2755A=	ENSP00000497658.1:n.*2755A=
ENST00000649781.2:c.2858A=	ENSP00000497203.1:p.Tyr953=
ENST00000685018.2:c.3041A=	ENSP00000510194.2:p.Tyr1014=
ENST00000687278.2:c.3041A=	ENSP00000509593.2:p.Tyr1014=
ENST00000699585.1:c.3041A=	ENSP00000514456.1:p.Tyr1014=
ENST00000699598.1:c.3041A=	ENSP00000514467.1:p.Tyr1014=
ENST00000699599.1:c.3041A=	ENSP00000514468.1:p.Tyr1014=
ENST00000699600.1:c.3041A=	ENSP00000514469.1:p.Tyr1014=
ENST00000699601.1:c.*1341A=	ENSP00000514470.1:n.*1341A=
ENST00000699602.1:c.3041A=	ENSP00000514471.1:p.Tyr1014=
ENST00000699604.1:c.*2865A=	ENSP00000514472.1:n.*2865A=
ENST00000699605.1:c.2615A=	ENSP00000514473.1:p.Tyr872=
ENST00000687278.1:c.632A=	ENSP00000509593.1:p.Tyr211=
ENST00000003084.11:c.3041A= MANE Select	ENSP00000003084.6:p.Tyr1014=
ENST00000647720.1:c.691A=
ENST00000648260.1:c.1823A=	ENSP00000497957.1:p.Tyr608=
ENST00000649406.1:c.2858A=	ENSP00000497965.1:p.Tyr953=
ENST00000649781.1:c.2858A=	ENSP00000497203.1:p.Tyr953=
ENST00000003084.10:c.3041A=	ENSP00000003084.6:p.Tyr1014=
ENST00000426809.5:c.2951A=	ENSP00000389119.1:p.Tyr984=
NM_000492.3:c.3041A= , LRG_663t1:c.3041A=	NP_000483.3:p.Tyr1014=
XM_011515751.1:c.3131A=	XP_011514053.1:p.Tyr1044=
XM_011515752.1:c.3131A=	XP_011514054.1:p.Tyr1044=
XM_011515753.1:c.2798A=	XP_011514055.1:p.Tyr933=
XM_011515754.1:c.2798A=	XP_011514056.1:p.Tyr933=
NM_000492.4:c.3041A= MANE Select	NP_000483.3:p.Tyr1014=