Canonical Allele Identifier: CA327106

Gene: CFTR

Linked Data

• dbSNP Id: rs397508519
• MyVariant Identifiers: chr7:g.117251731A>C (hg19) ; chr7:g.117611677A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611677A>C , CM000669.2:g.117611677A>C	GRCh38
NC_000007.13:g.117251731A>C , CM000669.1:g.117251731A>C	GRCh37
NC_000007.12:g.117038967A>C	NCBI36
NG_016465.4:g.150894A>C , LRG_663:g.150894A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3236A>C	ENSP00000497673.2:p.His1079Pro
ENST00000647978.2:c.*2950A>C	ENSP00000497658.1:n.*2950A>C
ENST00000649781.2:c.3053A>C	ENSP00000497203.1:p.His1018Pro
ENST00000685018.2:c.3236A>C	ENSP00000510194.2:p.His1079Pro
ENST00000687278.2:c.3236A>C	ENSP00000509593.2:p.His1079Pro
ENST00000699585.1:c.3236A>C	ENSP00000514456.1:p.His1079Pro
ENST00000699598.1:c.3236A>C	ENSP00000514467.1:p.His1079Pro
ENST00000699599.1:c.3236A>C	ENSP00000514468.1:p.His1079Pro
ENST00000699600.1:c.3236A>C	ENSP00000514469.1:p.His1079Pro
ENST00000699601.1:c.*1536A>C	ENSP00000514470.1:n.*1536A>C
ENST00000699602.1:c.3236A>C	ENSP00000514471.1:p.His1079Pro
ENST00000699604.1:c.*3060A>C	ENSP00000514472.1:n.*3060A>C
ENST00000699605.1:c.2810A>C	ENSP00000514473.1:p.His937Pro
ENST00000687278.1:c.827A>C	ENSP00000509593.1:p.His276Pro
ENST00000003084.11:c.3236A>C MANE Select	ENSP00000003084.6:p.His1079Pro
ENST00000647720.1:c.886A>C
ENST00000648260.1:c.2018A>C	ENSP00000497957.1:p.His673Pro
ENST00000649406.1:c.3053A>C	ENSP00000497965.1:p.His1018Pro
ENST00000649781.1:c.3053A>C	ENSP00000497203.1:p.His1018Pro
ENST00000003084.10:c.3236A>C	ENSP00000003084.6:p.His1079Pro
ENST00000426809.5:c.3146A>C	ENSP00000389119.1:p.His1049Pro
ENST00000468795.1:c.61A>C
NM_000492.3:c.3236A>C , LRG_663t1:c.3236A>C	NP_000483.3:p.His1079Pro
XM_011515751.1:c.3326A>C	XP_011514053.1:p.His1109Pro
XM_011515752.1:c.3326A>C	XP_011514054.1:p.His1109Pro
XM_011515753.1:c.2993A>C	XP_011514055.1:p.His998Pro
XM_011515754.1:c.2993A>C	XP_011514056.1:p.His998Pro
NM_000492.4:c.3236A>C MANE Select	NP_000483.3:p.His1079Pro