Canonical Allele Identifier: CA2684618011

Gene: CFTR

Linked Data

• gnomAD v4: 7-117509180-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117509180A>G , CM000669.2:g.117509180A>G	GRCh38
NC_000007.13:g.117149234A>G , CM000669.1:g.117149234A>G	GRCh37
NC_000007.12:g.116936470A>G	NCBI36
NG_016465.4:g.48397A>G , LRG_663:g.48397A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.273+38A>G	ENSP00000497673.2:n.273+38A>G
ENST00000647978.2:c.*170+38A>G	ENSP00000497658.1:n.*170+38A>G
ENST00000649781.2:c.273+38A>G	ENSP00000497203.1:n.273+38A>G
ENST00000649850.2:c.*208A>G	ENSP00000514457.1:n.*208A>G
ENST00000685018.2:c.273+38A>G	ENSP00000510194.2:n.273+38A>G
ENST00000687278.2:c.273+38A>G	ENSP00000509593.2:n.273+38A>G
ENST00000699585.1:c.273+38A>G	ENSP00000514456.1:n.273+38A>G
ENST00000699596.1:c.273+38A>G	ENSP00000514465.1:n.273+38A>G
ENST00000699597.1:c.273+38A>G	ENSP00000514466.1:n.273+38A>G
ENST00000699598.1:c.273+38A>G	ENSP00000514467.1:n.273+38A>G
ENST00000699599.1:c.273+38A>G	ENSP00000514468.1:n.273+38A>G
ENST00000699600.1:c.273+38A>G	ENSP00000514469.1:n.273+38A>G
ENST00000699601.1:c.273+38A>G	ENSP00000514470.1:n.273+38A>G
ENST00000699602.1:c.273+38A>G	ENSP00000514471.1:n.273+38A>G
ENST00000699604.1:c.*97+38A>G	ENSP00000514472.1:n.*97+38A>G
ENST00000699605.1:c.30+38A>G	ENSP00000514473.1:n.30+38A>G
ENST00000446805.2:c.30+38A>G	ENSP00000417012.1:n.30+38A>G
ENST00000003084.11:c.273+38A>G MANE Select	ENSP00000003084.6:n.273+38A>G
ENST00000647639.1:n.357+38A>G
ENST00000647978.1:c.*170+38A>G	ENSP00000497658.1:n.*170+38A>G
ENST00000648260.1:c.273+38A>G	ENSP00000497957.1:n.273+38A>G
ENST00000649406.1:c.273+38A>G	ENSP00000497965.1:n.273+38A>G
ENST00000649781.1:c.273+38A>G	ENSP00000497203.1:n.273+38A>G
ENST00000649850.1:n.468A>G
ENST00000673785.1:c.30+38A>G	ENSP00000501235.1:n.30+38A>G
ENST00000003084.10:c.273+38A>G	ENSP00000003084.6:n.273+38A>G
ENST00000426809.5:c.273+38A>G	ENSP00000389119.1:n.273+38A>G
ENST00000446805.1:c.30+38A>G	ENSP00000417012.1:n.30+38A>G
NM_000492.3:c.273+38A>G , LRG_663t1:c.273+38A>G	NP_000483.3:n.273+38A>G
XM_011515751.1:c.363+38A>G	XP_011514053.1:n.363+38A>G
XM_011515752.1:c.363+38A>G	XP_011514054.1:n.363+38A>G
XM_011515753.1:c.30+38A>G	XP_011514055.1:n.30+38A>G
XM_011515754.1:c.30+38A>G	XP_011514056.1:n.30+38A>G
NM_000492.4:c.273+38A>G MANE Select	NP_000483.3:n.273+38A>G