Canonical Allele Identifier: CA326408

Gene: CFTR

Linked Data

• dbSNP Id: rs397508160
• MyVariant Identifiers: chr7:g.117182040_117182041del (hg19) ; chr7:g.117541986_117541987del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117541986_117541987del , CM000669.2:g.117541986_117541987del	GRCh38
NC_000007.13:g.117182040_117182041del , CM000669.1:g.117182040_117182041del	GRCh37
NC_000007.12:g.116969276_116969277del	NCBI36
NG_016465.4:g.81203_81204del , LRG_663:g.81203_81204del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.1117-30_1117-29del	ENSP00000497673.2:n.1117-30_1117-29del
ENST00000647978.2:c.*1014-30_*1014-29del	ENSP00000497658.1:n.*1014-30_*1014-29del
ENST00000649781.2:c.1117-30_1117-29del	ENSP00000497203.1:n.1117-30_1117-29del
ENST00000685018.2:c.1117-30_1117-29del	ENSP00000510194.2:n.1117-30_1117-29del
ENST00000687278.2:c.1117-30_1117-29del	ENSP00000509593.2:n.1117-30_1117-29del
ENST00000699585.1:c.1117-30_1117-29del	ENSP00000514456.1:n.1117-30_1117-29del
ENST00000699596.1:c.1117-30_1117-29del	ENSP00000514465.1:n.1117-30_1117-29del
ENST00000699597.1:c.1117-30_1117-29del	ENSP00000514466.1:n.1117-30_1117-29del
ENST00000699598.1:c.1117-30_1117-29del	ENSP00000514467.1:n.1117-30_1117-29del
ENST00000699599.1:c.1117-30_1117-29del	ENSP00000514468.1:n.1117-30_1117-29del
ENST00000699600.1:c.1117-30_1117-29del	ENSP00000514469.1:n.1117-30_1117-29del
ENST00000699601.1:c.1117-30_1117-29del	ENSP00000514470.1:n.1117-30_1117-29del
ENST00000699602.1:c.1117-30_1117-29del	ENSP00000514471.1:n.1117-30_1117-29del
ENST00000699604.1:c.*941-30_*941-29del	ENSP00000514472.1:n.*941-30_*941-29del
ENST00000699605.1:c.874-30_874-29del	ENSP00000514473.1:n.874-30_874-29del
ENST00000003084.11:c.1117-30_1117-29del MANE Select	ENSP00000003084.6:n.1117-30_1117-29del
ENST00000647978.1:c.*1014-30_*1014-29del	ENSP00000497658.1:n.*1014-30_*1014-29del
ENST00000648260.1:c.1117-30_1117-29del	ENSP00000497957.1:n.1117-30_1117-29del
ENST00000649406.1:c.1117-30_1117-29del	ENSP00000497965.1:n.1117-30_1117-29del
ENST00000649781.1:c.1117-30_1117-29del	ENSP00000497203.1:n.1117-30_1117-29del
ENST00000673785.1:c.874-30_874-29del	ENSP00000501235.1:n.874-30_874-29del
ENST00000003084.10:c.1117-30_1117-29del	ENSP00000003084.6:n.1117-30_1117-29del
ENST00000426809.5:c.1027-30_1027-29del	ENSP00000389119.1:n.1027-30_1027-29del
NM_000492.3:c.1117-30_1117-29del , LRG_663t1:c.1117-30_1117-29del	NP_000483.3:n.1117-30_1117-29del
XM_011515751.1:c.1207-30_1207-29del	XP_011514053.1:n.1207-30_1207-29del
XM_011515752.1:c.1207-30_1207-29del	XP_011514054.1:n.1207-30_1207-29del
XM_011515753.1:c.874-30_874-29del	XP_011514055.1:n.874-30_874-29del
XM_011515754.1:c.874-30_874-29del	XP_011514056.1:n.874-30_874-29del
NM_000492.4:c.1117-30_1117-29del MANE Select	NP_000483.3:n.1117-30_1117-29del