Canonical Allele Identifier: CA368996066

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117267602G>C (hg19) ; chr7:g.117627548G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117627548G>C , CM000669.2:g.117627548G>C	GRCh38
NC_000007.13:g.117267602G>C , CM000669.1:g.117267602G>C	GRCh37
NC_000007.12:g.117054838G>C	NCBI36
NG_016465.4:g.166765G>C , LRG_663:g.166765G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3495G>C	ENSP00000497673.2:p.Lys1165Asn
ENST00000647978.2:c.*3209G>C	ENSP00000497658.1:n.*3209G>C
ENST00000649781.2:c.3312G>C	ENSP00000497203.1:p.Lys1104Asn
ENST00000685018.2:c.3495G>C	ENSP00000510194.2:p.Lys1165Asn
ENST00000687278.2:c.*148G>C	ENSP00000509593.2:n.*148G>C
ENST00000699585.1:c.3495G>C	ENSP00000514456.1:p.Lys1165Asn
ENST00000699598.1:c.3495G>C	ENSP00000514467.1:p.Lys1165Asn
ENST00000699599.1:c.3495G>C	ENSP00000514468.1:p.Lys1165Asn
ENST00000699600.1:c.*156G>C	ENSP00000514469.1:n.*156G>C
ENST00000699601.1:c.*1870G>C	ENSP00000514470.1:n.*1870G>C
ENST00000699602.1:c.3489G>C	ENSP00000514471.1:p.Lys1163Asn
ENST00000699604.1:c.*3319G>C	ENSP00000514472.1:n.*3319G>C
ENST00000699605.1:c.3069G>C	ENSP00000514473.1:p.Lys1023Asn
ENST00000685018.1:c.243G>C	ENSP00000510194.1:p.Lys81Asn
ENST00000687278.1:c.1282G>C	ENSP00000509593.1:n.1282G>C
ENST00000689011.1:c.77G>C
ENST00000003084.11:c.3495G>C MANE Select	ENSP00000003084.6:p.Lys1165Asn
ENST00000647720.1:c.1145G>C
ENST00000648260.1:c.2277G>C	ENSP00000497957.1:p.Lys759Asn
ENST00000649406.1:c.3312G>C	ENSP00000497965.1:p.Lys1104Asn
ENST00000649781.1:c.3312G>C	ENSP00000497203.1:p.Lys1104Asn
ENST00000003084.10:c.3495G>C	ENSP00000003084.6:p.Lys1165Asn
ENST00000426809.5:c.3405G>C	ENSP00000389119.1:p.Lys1135Asn
ENST00000468795.1:c.320G>C
NM_000492.3:c.3495G>C , LRG_663t1:c.3495G>C	NP_000483.3:p.Lys1165Asn
XM_011515751.1:c.3585G>C	XP_011514053.1:p.Lys1195Asn
XM_011515752.1:c.3585G>C	XP_011514054.1:p.Lys1195Asn
XM_011515753.1:c.3252G>C	XP_011514055.1:p.Lys1084Asn
XM_011515754.1:c.3252G>C	XP_011514056.1:p.Lys1084Asn
NM_000492.4:c.3495G>C MANE Select	NP_000483.3:p.Lys1165Asn