Canonical Allele Identifier: CA457227561

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117234995T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117594941T>C , CM000669.2:g.117594941T>C	GRCh38
NC_000007.13:g.117234995T>C , CM000669.1:g.117234995T>C	GRCh37
NC_000007.12:g.117022231T>C	NCBI36
NG_016465.4:g.134158T>C , LRG_663:g.134158T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.2502T>C	ENSP00000497673.2:p.Phe834=
ENST00000647978.2:c.*2216T>C	ENSP00000497658.1:n.*2216T>C
ENST00000649781.2:c.2319T>C	ENSP00000497203.1:p.Phe773=
ENST00000685018.2:c.2502T>C	ENSP00000510194.2:p.Phe834=
ENST00000687278.2:c.2502T>C	ENSP00000509593.2:p.Phe834=
ENST00000699585.1:c.2502T>C	ENSP00000514456.1:p.Phe834=
ENST00000699598.1:c.2502T>C	ENSP00000514467.1:p.Phe834=
ENST00000699599.1:c.2502T>C	ENSP00000514468.1:p.Phe834=
ENST00000699600.1:c.2502T>C	ENSP00000514469.1:p.Phe834=
ENST00000699601.1:c.*802T>C	ENSP00000514470.1:n.*802T>C
ENST00000699602.1:c.2502T>C	ENSP00000514471.1:p.Phe834=
ENST00000699604.1:c.*2326T>C	ENSP00000514472.1:n.*2326T>C
ENST00000699605.1:c.2076T>C	ENSP00000514473.1:p.Phe692=
ENST00000687278.1:c.93T>C	ENSP00000509593.1:p.Phe31=
ENST00000003084.11:c.2502T>C MANE Select	ENSP00000003084.6:p.Phe834=
ENST00000647720.1:c.152T>C
ENST00000647978.1:c.*2216T>C	ENSP00000497658.1:n.*2216T>C
ENST00000648260.1:c.1402-7885T>C	ENSP00000497957.1:n.1402-7885T>C
ENST00000649406.1:c.2319T>C	ENSP00000497965.1:p.Phe773=
ENST00000649781.1:c.2319T>C	ENSP00000497203.1:p.Phe773=
ENST00000003084.10:c.2502T>C	ENSP00000003084.6:p.Phe834=
ENST00000426809.5:c.2412T>C	ENSP00000389119.1:p.Phe804=
NM_000492.3:c.2502T>C , LRG_663t1:c.2502T>C	NP_000483.3:p.Phe834=
XM_011515751.1:c.2592T>C	XP_011514053.1:p.Phe864=
XM_011515752.1:c.2592T>C	XP_011514054.1:p.Phe864=
XM_011515753.1:c.2259T>C	XP_011514055.1:p.Phe753=
XM_011515754.1:c.2259T>C	XP_011514056.1:p.Phe753=
NM_000492.4:c.2502T>C MANE Select	NP_000483.3:p.Phe834=