Canonical Allele Identifier: CA164937138

Gene: CFTR

Linked Data

• dbSNP Id: rs111155389
• MyVariant Identifiers: chr7:g.117149196_117149197insCCCTA (hg19) ; chr7:g.117509142_117509143insCCCTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117509142_117509143insCCCTA , CM000669.2:g.117509142_117509143insCCCTA	GRCh38
NC_000007.13:g.117149196_117149197insCCCTA , CM000669.1:g.117149196_117149197insCCCTA	GRCh37
NC_000007.12:g.116936432_116936433insCCCTA	NCBI36
NG_016465.4:g.48359_48360insCCCTA , LRG_663:g.48359_48360insCCCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.273_273+1insCCCTA	ENSP00000497673.2:n.273_273+1insCCCTA
ENST00000647978.2:c.*170_*170+1insCCCTA	ENSP00000497658.1:n.*170_*170+1insCCCTA
ENST00000649781.2:c.273_273+1insCCCTA	ENSP00000497203.1:n.273_273+1insCCCTA
ENST00000649850.2:c.*170_*171insCCCTA	ENSP00000514457.1:n.*170_*171insCCCTA
ENST00000685018.2:c.273_273+1insCCCTA	ENSP00000510194.2:n.273_273+1insCCCTA
ENST00000687278.2:c.273_273+1insCCCTA	ENSP00000509593.2:n.273_273+1insCCCTA
ENST00000699585.1:c.273_273+1insCCCTA	ENSP00000514456.1:n.273_273+1insCCCTA
ENST00000699596.1:c.273_273+1insCCCTA	ENSP00000514465.1:n.273_273+1insCCCTA
ENST00000699597.1:c.273_273+1insCCCTA	ENSP00000514466.1:n.273_273+1insCCCTA
ENST00000699598.1:c.273_273+1insCCCTA	ENSP00000514467.1:n.273_273+1insCCCTA
ENST00000699599.1:c.273_273+1insCCCTA	ENSP00000514468.1:n.273_273+1insCCCTA
ENST00000699600.1:c.273_273+1insCCCTA	ENSP00000514469.1:n.273_273+1insCCCTA
ENST00000699601.1:c.273_273+1insCCCTA	ENSP00000514470.1:n.273_273+1insCCCTA
ENST00000699602.1:c.273_273+1insCCCTA	ENSP00000514471.1:n.273_273+1insCCCTA
ENST00000699604.1:c.*97_*97+1insCCCTA	ENSP00000514472.1:n.*97_*97+1insCCCTA
ENST00000699605.1:c.30_30+1insCCCTA	ENSP00000514473.1:n.30_30+1insCCCTA
ENST00000446805.2:c.30_30+1insCCCTA	ENSP00000417012.1:n.30_30+1insCCCTA
ENST00000003084.11:c.273_273+1insCCCTA MANE Select	ENSP00000003084.6:n.273_273+1insCCCTA
ENST00000647639.1:n.357_357+1insCCCTA
ENST00000647978.1:c.*170_*170+1insCCCTA	ENSP00000497658.1:n.*170_*170+1insCCCTA
ENST00000648260.1:c.273_273+1insCCCTA	ENSP00000497957.1:n.273_273+1insCCCTA
ENST00000649406.1:c.273_273+1insCCCTA	ENSP00000497965.1:n.273_273+1insCCCTA
ENST00000649781.1:c.273_273+1insCCCTA	ENSP00000497203.1:n.273_273+1insCCCTA
ENST00000649850.1:n.430_431insCCCTA
ENST00000673785.1:c.30_30+1insCCCTA	ENSP00000501235.1:n.30_30+1insCCCTA
ENST00000003084.10:c.273_273+1insCCCTA	ENSP00000003084.6:n.273_273+1insCCCTA
ENST00000426809.5:c.273_273+1insCCCTA	ENSP00000389119.1:n.273_273+1insCCCTA
ENST00000446805.1:c.30_30+1insCCCTA	ENSP00000417012.1:n.30_30+1insCCCTA
NM_000492.3:c.273_273+1insCCCTA , LRG_663t1:c.273_273+1insCCCTA	NP_000483.3:n.273_273+1insCCCTA
XM_011515751.1:c.363_363+1insCCCTA	XP_011514053.1:n.363_363+1insCCCTA
XM_011515752.1:c.363_363+1insCCCTA	XP_011514054.1:n.363_363+1insCCCTA
XM_011515753.1:c.30_30+1insCCCTA	XP_011514055.1:n.30_30+1insCCCTA
XM_011515754.1:c.30_30+1insCCCTA	XP_011514056.1:n.30_30+1insCCCTA
NM_000492.4:c.273_273+1insCCCTA MANE Select	NP_000483.3:n.273_273+1insCCCTA