Canonical Allele Identifier: CA2684617326

Gene: CFTR

Linked Data

• gnomAD v4: 7-117531001-GGCTTATGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117531002_117531009del , CM000669.2:g.117531002_117531009del	GRCh38
NC_000007.13:g.117171056_117171063del , CM000669.1:g.117171056_117171063del	GRCh37
NC_000007.12:g.116958292_116958299del	NCBI36
NG_016465.4:g.70219_70226del , LRG_663:g.70219_70226del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.377_384del	ENSP00000497673.2:p.Gly126AlafsTer30
ENST00000647978.2:c.*274_*281del	ENSP00000497658.1:n.*274_*281del
ENST00000649781.2:c.377_384del	ENSP00000497203.1:p.Gly126AlafsTer30
ENST00000685018.2:c.377_384del	ENSP00000510194.2:p.Gly126AlafsTer30
ENST00000687278.2:c.377_384del	ENSP00000509593.2:p.Gly126AlafsTer30
ENST00000699585.1:c.377_384del	ENSP00000514456.1:p.Gly126AlafsTer30
ENST00000699596.1:c.377_384del	ENSP00000514465.1:p.Gly126AlafsTer30
ENST00000699597.1:c.377_384del	ENSP00000514466.1:p.Gly126AlafsTer30
ENST00000699598.1:c.377_384del	ENSP00000514467.1:p.Gly126AlafsTer30
ENST00000699599.1:c.377_384del	ENSP00000514468.1:p.Gly126AlafsTer30
ENST00000699600.1:c.377_384del	ENSP00000514469.1:p.Gly126AlafsTer30
ENST00000699601.1:c.377_384del	ENSP00000514470.1:p.Gly126AlafsTer30
ENST00000699602.1:c.377_384del	ENSP00000514471.1:p.Gly126AlafsTer30
ENST00000699604.1:c.*201_*208del	ENSP00000514472.1:n.*201_*208del
ENST00000699605.1:c.134_141del	ENSP00000514473.1:p.Gly45AlafsTer30
ENST00000003084.11:c.377_384del MANE Select	ENSP00000003084.6:p.Gly126AlafsTer30
ENST00000647978.1:c.*274_*281del	ENSP00000497658.1:n.*274_*281del
ENST00000648260.1:c.377_384del	ENSP00000497957.1:p.Gly126AlafsTer30
ENST00000649406.1:c.377_384del	ENSP00000497965.1:p.Gly126AlafsTer30
ENST00000649781.1:c.377_384del	ENSP00000497203.1:p.Gly126AlafsTer30
ENST00000673785.1:c.134_141del	ENSP00000501235.1:p.Gly45AlafsTer30
ENST00000003084.10:c.377_384del	ENSP00000003084.6:p.Gly126AlafsTer30
ENST00000426809.5:c.377_384del	ENSP00000389119.1:p.Gly126AlafsTer30
NM_000492.3:c.377_384del , LRG_663t1:c.377_384del	NP_000483.3:p.Gly126AlafsTer30
XM_011515751.1:c.467_474del	XP_011514053.1:p.Gly156AlafsTer30
XM_011515752.1:c.467_474del	XP_011514054.1:p.Gly156AlafsTer30
XM_011515753.1:c.134_141del	XP_011514055.1:p.Gly45AlafsTer30
XM_011515754.1:c.134_141del	XP_011514056.1:p.Gly45AlafsTer30
NM_000492.4:c.377_384del MANE Select	NP_000483.3:p.Gly126AlafsTer30