Canonical Allele Identifier: CA832121291

Gene: CFTR

Linked Data

• dbSNP Id: rs1454104569
• gnomAD v3: 7-117614535-TAGG-T
• gnomAD v4: 7-117614535-TAGG-T
• MyVariant Identifiers: chr7:g.117254590_117254592del (hg19) ; chr7:g.117614536_117614538del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117614538_117614540del , CM000669.2:g.117614538_117614540del	GRCh38
NC_000007.13:g.117254592_117254594del , CM000669.1:g.117254592_117254594del	GRCh37
NC_000007.12:g.117041828_117041830del	NCBI36
NG_016465.4:g.153755_153757del , LRG_663:g.153755_153757del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3368-75_3368-73del	ENSP00000497673.2:n.3368-75_3368-73del
ENST00000647978.2:c.*3082-75_*3082-73del	ENSP00000497658.1:n.*3082-75_*3082-73del
ENST00000649781.2:c.3185-75_3185-73del	ENSP00000497203.1:n.3185-75_3185-73del
ENST00000685018.2:c.3368-75_3368-73del	ENSP00000510194.2:n.3368-75_3368-73del
ENST00000687278.2:c.3368-75_3368-73del	ENSP00000509593.2:n.3368-75_3368-73del
ENST00000699585.1:c.3368-75_3368-73del	ENSP00000514456.1:n.3368-75_3368-73del
ENST00000699598.1:c.3368-75_3368-73del	ENSP00000514467.1:n.3368-75_3368-73del
ENST00000699599.1:c.3368-75_3368-73del	ENSP00000514468.1:n.3368-75_3368-73del
ENST00000699600.1:c.3368-75_3368-73del	ENSP00000514469.1:n.3368-75_3368-73del
ENST00000699601.1:c.*1668_*1670del
ENST00000699602.1:c.3368-81_3368-79del	ENSP00000514471.1:n.3368-81_3368-79del
ENST00000699604.1:c.*3192-75_*3192-73del	ENSP00000514472.1:n.*3192-75_*3192-73del
ENST00000699605.1:c.2942-75_2942-73del	ENSP00000514473.1:n.2942-75_2942-73del
ENST00000685018.1:c.116-75_116-73del	ENSP00000510194.1:n.116-75_116-73del
ENST00000687278.1:c.959-75_959-73del	ENSP00000509593.1:n.959-75_959-73del
ENST00000003084.11:c.3368-75_3368-73del MANE Select	ENSP00000003084.6:n.3368-75_3368-73del
ENST00000647720.1:c.1018-75_1018-73del
ENST00000648260.1:c.2150-75_2150-73del	ENSP00000497957.1:n.2150-75_2150-73del
ENST00000649406.1:c.3185-75_3185-73del	ENSP00000497965.1:n.3185-75_3185-73del
ENST00000649781.1:c.3185-75_3185-73del	ENSP00000497203.1:n.3185-75_3185-73del
ENST00000003084.10:c.3368-75_3368-73del	ENSP00000003084.6:n.3368-75_3368-73del
ENST00000426809.5:c.3278-75_3278-73del	ENSP00000389119.1:n.3278-75_3278-73del
ENST00000468795.1:c.193-75_193-73del
NM_000492.3:c.3368-75_3368-73del , LRG_663t1:c.3368-75_3368-73del	NP_000483.3:n.3368-75_3368-73del
XM_011515751.1:c.3458-75_3458-73del	XP_011514053.1:n.3458-75_3458-73del
XM_011515752.1:c.3458-75_3458-73del	XP_011514054.1:n.3458-75_3458-73del
XM_011515753.1:c.3125-75_3125-73del	XP_011514055.1:n.3125-75_3125-73del
XM_011515754.1:c.3125-75_3125-73del	XP_011514056.1:n.3125-75_3125-73del
NM_000492.4:c.3368-75_3368-73del MANE Select	NP_000483.3:n.3368-75_3368-73del