Canonical Allele Identifier: CA164975049

Gene: CFTR

Linked Data

• dbSNP Id: rs574102779
• gnomAD v2: 7-117264714-A-G
• gnomAD v3: 7-117624660-A-G
• gnomAD v4: 7-117624660-A-G
• MyVariant Identifiers: chr7:g.117264714A>G (hg19) ; chr7:g.117624660A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117624660A>G , CM000669.2:g.117624660A>G	GRCh38
NC_000007.13:g.117264714A>G , CM000669.1:g.117264714A>G	GRCh37
NC_000007.12:g.117051950A>G	NCBI36
NG_016465.4:g.163877A>G , LRG_663:g.163877A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3469-2862A>G	ENSP00000497673.2:n.3469-2862A>G
ENST00000647978.2:c.*3183-2862A>G	ENSP00000497658.1:n.*3183-2862A>G
ENST00000649781.2:c.3286-2862A>G	ENSP00000497203.1:n.3286-2862A>G
ENST00000685018.2:c.3469-2862A>G	ENSP00000510194.2:n.3469-2862A>G
ENST00000687278.2:c.3469-1344A>G	ENSP00000509593.2:n.3469-1344A>G
ENST00000699585.1:c.3469-2862A>G	ENSP00000514456.1:n.3469-2862A>G
ENST00000699598.1:c.3469-2862A>G	ENSP00000514467.1:n.3469-2862A>G
ENST00000699599.1:c.3469-2862A>G	ENSP00000514468.1:n.3469-2862A>G
ENST00000699600.1:c.3469-1344A>G	ENSP00000514469.1:n.3469-1344A>G
ENST00000699601.1:c.*1844-2862A>G	ENSP00000514470.1:n.*1844-2862A>G
ENST00000699602.1:c.3463-2862A>G	ENSP00000514471.1:n.3463-2862A>G
ENST00000699604.1:c.*3293-2862A>G	ENSP00000514472.1:n.*3293-2862A>G
ENST00000699605.1:c.3043-2862A>G	ENSP00000514473.1:n.3043-2862A>G
ENST00000685018.1:c.217-2862A>G	ENSP00000510194.1:n.217-2862A>G
ENST00000687278.1:c.1060-1344A>G	ENSP00000509593.1:n.1060-1344A>G
ENST00000689011.1:c.51-2862A>G
ENST00000003084.11:c.3469-2862A>G MANE Select	ENSP00000003084.6:n.3469-2862A>G
ENST00000647720.1:c.1119-2862A>G
ENST00000648260.1:c.2251-2862A>G	ENSP00000497957.1:n.2251-2862A>G
ENST00000649406.1:c.3286-2862A>G	ENSP00000497965.1:n.3286-2862A>G
ENST00000649781.1:c.3286-2862A>G	ENSP00000497203.1:n.3286-2862A>G
ENST00000003084.10:c.3469-2862A>G	ENSP00000003084.6:n.3469-2862A>G
ENST00000426809.5:c.3379-2862A>G	ENSP00000389119.1:n.3379-2862A>G
ENST00000468795.1:c.294-2862A>G
NM_000492.3:c.3469-2862A>G , LRG_663t1:c.3469-2862A>G	NP_000483.3:n.3469-2862A>G
XM_011515751.1:c.3559-2862A>G	XP_011514053.1:n.3559-2862A>G
XM_011515752.1:c.3559-2862A>G	XP_011514054.1:n.3559-2862A>G
XM_011515753.1:c.3226-2862A>G	XP_011514055.1:n.3226-2862A>G
XM_011515754.1:c.3226-2862A>G	XP_011514056.1:n.3226-2862A>G
NM_000492.4:c.3469-2862A>G MANE Select	NP_000483.3:n.3469-2862A>G