Canonical Allele Identifier: CA325701

Gene: CFTR

Linked Data

• ClinVar Variation Id: 35846
• ClinVar RCV Id: RCV000029501 ; RCV001004421
• dbSNP Id: rs74467662
• MyVariant Identifiers: chr7:g.117149199A>C (hg19) ; chr7:g.117509145A>C (hg38)
• PubMed: PMID:9150159 ; PMID:11388756 ; PMID:23974870

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117509145A>C , CM000669.2:g.117509145A>C	GRCh38
NC_000007.13:g.117149199A>C , CM000669.1:g.117149199A>C	GRCh37
NC_000007.12:g.116936435A>C	NCBI36
NG_016465.4:g.48362A>C , LRG_663:g.48362A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.273+3A>C	ENSP00000497673.2:n.273+3A>C
ENST00000647978.2:c.*170+3A>C	ENSP00000497658.1:n.*170+3A>C
ENST00000649781.2:c.273+3A>C	ENSP00000497203.1:n.273+3A>C
ENST00000649850.2:c.*173A>C	ENSP00000514457.1:n.*173A>C
ENST00000685018.2:c.273+3A>C	ENSP00000510194.2:n.273+3A>C
ENST00000687278.2:c.273+3A>C	ENSP00000509593.2:n.273+3A>C
ENST00000699585.1:c.273+3A>C	ENSP00000514456.1:n.273+3A>C
ENST00000699596.1:c.273+3A>C	ENSP00000514465.1:n.273+3A>C
ENST00000699597.1:c.273+3A>C	ENSP00000514466.1:n.273+3A>C
ENST00000699598.1:c.273+3A>C	ENSP00000514467.1:n.273+3A>C
ENST00000699599.1:c.273+3A>C	ENSP00000514468.1:n.273+3A>C
ENST00000699600.1:c.273+3A>C	ENSP00000514469.1:n.273+3A>C
ENST00000699601.1:c.273+3A>C	ENSP00000514470.1:n.273+3A>C
ENST00000699602.1:c.273+3A>C	ENSP00000514471.1:n.273+3A>C
ENST00000699604.1:c.*97+3A>C	ENSP00000514472.1:n.*97+3A>C
ENST00000699605.1:c.30+3A>C	ENSP00000514473.1:n.30+3A>C
ENST00000446805.2:c.30+3A>C	ENSP00000417012.1:n.30+3A>C
ENST00000003084.11:c.273+3A>C MANE Select	ENSP00000003084.6:n.273+3A>C
ENST00000647639.1:n.357+3A>C
ENST00000647978.1:c.*170+3A>C	ENSP00000497658.1:n.*170+3A>C
ENST00000648260.1:c.273+3A>C	ENSP00000497957.1:n.273+3A>C
ENST00000649406.1:c.273+3A>C	ENSP00000497965.1:n.273+3A>C
ENST00000649781.1:c.273+3A>C	ENSP00000497203.1:n.273+3A>C
ENST00000649850.1:n.433A>C
ENST00000673785.1:c.30+3A>C	ENSP00000501235.1:n.30+3A>C
ENST00000003084.10:c.273+3A>C	ENSP00000003084.6:n.273+3A>C
ENST00000426809.5:c.273+3A>C	ENSP00000389119.1:n.273+3A>C
ENST00000446805.1:c.30+3A>C	ENSP00000417012.1:n.30+3A>C
NM_000492.3:c.273+3A>C , LRG_663t1:c.273+3A>C	NP_000483.3:n.273+3A>C
XM_011515751.1:c.363+3A>C	XP_011514053.1:n.363+3A>C
XM_011515752.1:c.363+3A>C	XP_011514054.1:n.363+3A>C
XM_011515753.1:c.30+3A>C	XP_011514055.1:n.30+3A>C
XM_011515754.1:c.30+3A>C	XP_011514056.1:n.30+3A>C
NM_000492.4:c.273+3A>C MANE Select	NP_000483.3:n.273+3A>C