Canonical Allele Identifier: CA577215198

Gene: CFTR

Linked Data

• dbSNP Id: rs1351041821
• gnomAD v2: 7-117182163-GTCAGAATTTTTAAAAAATTGTTTGCTCTAAACACCTAACTGTTTTCTTCT-G
• gnomAD v3: 7-117542109-GTCAGAATTTTTAAAAAATTGTTTGCTCTAAACACCTAACTGTTTTCTTCT-G
• gnomAD v4: 7-117542109-GTCAGAATTTTTAAAAAATTGTTTGCTCTAAACACCTAACTGTTTTCTTCT-G
• MyVariant Identifiers: chr7:g.117182164_117182213del (hg19) ; chr7:g.117542110_117542159del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117542111_117542160del , CM000669.2:g.117542111_117542160del	GRCh38
NC_000007.13:g.117182165_117182214del , CM000669.1:g.117182165_117182214del	GRCh37
NC_000007.12:g.116969401_116969450del	NCBI36
NG_016465.4:g.81328_81377del , LRG_663:g.81328_81377del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.1209+3_1209+52del	ENSP00000497673.2:n.1209+3_1209+52del
ENST00000647978.2:c.*1106+3_*1106+52del	ENSP00000497658.1:n.*1106+3_*1106+52del
ENST00000649781.2:c.1209+3_1209+52del	ENSP00000497203.1:n.1209+3_1209+52del
ENST00000685018.2:c.1209+3_1209+52del	ENSP00000510194.2:n.1209+3_1209+52del
ENST00000687278.2:c.1209+3_1209+52del	ENSP00000509593.2:n.1209+3_1209+52del
ENST00000699585.1:c.1209+3_1209+52del	ENSP00000514456.1:n.1209+3_1209+52del
ENST00000699596.1:c.1209+3_1209+52del	ENSP00000514465.1:n.1209+3_1209+52del
ENST00000699597.1:c.1209+3_1209+52del	ENSP00000514466.1:n.1209+3_1209+52del
ENST00000699598.1:c.1209+3_1209+52del	ENSP00000514467.1:n.1209+3_1209+52del
ENST00000699599.1:c.1209+3_1209+52del	ENSP00000514468.1:n.1209+3_1209+52del
ENST00000699600.1:c.1209+3_1209+52del	ENSP00000514469.1:n.1209+3_1209+52del
ENST00000699601.1:c.1209+3_1209+52del	ENSP00000514470.1:n.1209+3_1209+52del
ENST00000699602.1:c.1209+3_1209+52del	ENSP00000514471.1:n.1209+3_1209+52del
ENST00000699604.1:c.*1033+3_*1033+52del	ENSP00000514472.1:n.*1033+3_*1033+52del
ENST00000699605.1:c.966+3_966+52del	ENSP00000514473.1:n.966+3_966+52del
ENST00000003084.11:c.1209+3_1209+52del MANE Select	ENSP00000003084.6:n.1209+3_1209+52del
ENST00000647978.1:c.*1106+3_*1106+52del	ENSP00000497658.1:n.*1106+3_*1106+52del
ENST00000648260.1:c.1209+3_1209+52del	ENSP00000497957.1:n.1209+3_1209+52del
ENST00000649406.1:c.1209+3_1209+52del	ENSP00000497965.1:n.1209+3_1209+52del
ENST00000649781.1:c.1209+3_1209+52del	ENSP00000497203.1:n.1209+3_1209+52del
ENST00000673785.1:c.966+3_966+52del	ENSP00000501235.1:n.966+3_966+52del
ENST00000003084.10:c.1209+3_1209+52del	ENSP00000003084.6:n.1209+3_1209+52del
ENST00000426809.5:c.1119+3_1119+52del	ENSP00000389119.1:n.1119+3_1119+52del
NM_000492.3:c.1209+3_1209+52del , LRG_663t1:c.1209+3_1209+52del	NP_000483.3:n.1209+3_1209+52del
XM_011515751.1:c.1299+3_1299+52del	XP_011514053.1:n.1299+3_1299+52del
XM_011515752.1:c.1299+3_1299+52del	XP_011514054.1:n.1299+3_1299+52del
XM_011515753.1:c.966+3_966+52del	XP_011514055.1:n.966+3_966+52del
XM_011515754.1:c.966+3_966+52del	XP_011514056.1:n.966+3_966+52del
NM_000492.4:c.1209+3_1209+52del MANE Select	NP_000483.3:n.1209+3_1209+52del