Canonical Allele Identifier: CA2580076278

Gene: CFTR

Linked Data

• ClinVar Variation Id: 1705998
• ClinVar RCV Id: RCV002284528

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117530913_117530921del , CM000669.2:g.117530913_117530921del	GRCh38
NC_000007.13:g.117170967_117170975del , CM000669.1:g.117170967_117170975del	GRCh37
NC_000007.12:g.116958203_116958211del	NCBI36
NG_016465.4:g.70130_70138del , LRG_663:g.70130_70138del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.288_296del	ENSP00000497673.2:p.Val97_Pro99del
ENST00000647978.2:c.*185_*193del	ENSP00000497658.1:n.*185_*193del
ENST00000649781.2:c.288_296del	ENSP00000497203.1:p.Val97_Pro99del
ENST00000685018.2:c.288_296del	ENSP00000510194.2:p.Val97_Pro99del
ENST00000687278.2:c.288_296del	ENSP00000509593.2:p.Val97_Pro99del
ENST00000699585.1:c.288_296del	ENSP00000514456.1:p.Val97_Pro99del
ENST00000699596.1:c.288_296del	ENSP00000514465.1:p.Val97_Pro99del
ENST00000699597.1:c.288_296del	ENSP00000514466.1:p.Val97_Pro99del
ENST00000699598.1:c.288_296del	ENSP00000514467.1:p.Val97_Pro99del
ENST00000699599.1:c.288_296del	ENSP00000514468.1:p.Val97_Pro99del
ENST00000699600.1:c.288_296del	ENSP00000514469.1:p.Val97_Pro99del
ENST00000699601.1:c.288_296del	ENSP00000514470.1:p.Val97_Pro99del
ENST00000699602.1:c.288_296del	ENSP00000514471.1:p.Val97_Pro99del
ENST00000699604.1:c.*112_*120del	ENSP00000514472.1:n.*112_*120del
ENST00000699605.1:c.45_53del	ENSP00000514473.1:p.Val16_Pro18del
ENST00000446805.2:c.45_53del	ENSP00000417012.1:p.Val16_Pro18del
ENST00000003084.11:c.288_296del MANE Select	ENSP00000003084.6:p.Val97_Pro99del
ENST00000647978.1:c.*185_*193del	ENSP00000497658.1:n.*185_*193del
ENST00000648260.1:c.288_296del	ENSP00000497957.1:p.Val97_Pro99del
ENST00000649406.1:c.288_296del	ENSP00000497965.1:p.Val97_Pro99del
ENST00000649781.1:c.288_296del	ENSP00000497203.1:p.Val97_Pro99del
ENST00000673785.1:c.45_53del	ENSP00000501235.1:p.Val16_Pro18del
ENST00000003084.10:c.288_296del	ENSP00000003084.6:p.Val97_Pro99del
ENST00000426809.5:c.288_296del	ENSP00000389119.1:p.Val97_Pro99del
ENST00000446805.1:c.45_53del	ENSP00000417012.1:p.Val16_Pro18del
NM_000492.3:c.288_296del , LRG_663t1:c.288_296del	NP_000483.3:p.Val97_Pro99del
XM_011515751.1:c.378_386del	XP_011514053.1:p.Val127_Pro129del
XM_011515752.1:c.378_386del	XP_011514054.1:p.Val127_Pro129del
XM_011515753.1:c.45_53del	XP_011514055.1:p.Val16_Pro18del
XM_011515754.1:c.45_53del	XP_011514056.1:p.Val16_Pro18del
NM_000492.4:c.288_296del MANE Select	NP_000483.3:p.Val97_Pro99del