Canonical Allele Identifier: CA1737421150

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117664462_117664466delinsTAATG , CM000669.2:g.117664462_117664466delinsTAATG	GRCh38
NC_000007.13:g.117304516_117304520delinsTAATG , CM000669.1:g.117304516_117304520delinsTAATG	GRCh37
NC_000007.12:g.117091752_117091756delinsTAATG	NCBI36
NG_016465.4:g.203679_203683delinsTAATG , LRG_663:g.203679_203683delinsTAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.*173-226_*173-222delinsTAATG	ENSP00000497673.2:n.*173-226_*173-222delinsTAATG
ENST00000647978.2:c.*3678-226_*3678-222delinsTAATG	ENSP00000497658.1:n.*3678-226_*3678-222delinsTAATG
ENST00000649781.2:c.3781-226_3781-222delinsTAATG	ENSP00000497203.1:n.3781-226_3781-222delinsTAATG
ENST00000685018.2:c.*177-226_*177-222delinsTAATG	ENSP00000510194.2:n.*177-226_*177-222delinsTAATG
ENST00000687278.2:c.*617-226_*617-222delinsTAATG	ENSP00000509593.2:n.*617-226_*617-222delinsTAATG
ENST00000699585.1:c.*173-226_*173-222delinsTAATG	ENSP00000514456.1:n.*173-226_*173-222delinsTAATG
ENST00000699598.1:c.3964-226_3964-222delinsTAATG	ENSP00000514467.1:n.3964-226_3964-222delinsTAATG
ENST00000699599.1:c.*177-226_*177-222delinsTAATG	ENSP00000514468.1:n.*177-226_*177-222delinsTAATG
ENST00000699600.1:c.*625-226_*625-222delinsTAATG	ENSP00000514469.1:n.*625-226_*625-222delinsTAATG
ENST00000699601.1:c.*2339-226_*2339-222delinsTAATG	ENSP00000514470.1:n.*2339-226_*2339-222delinsTAATG
ENST00000699602.1:c.3958-226_3958-222delinsTAATG	ENSP00000514471.1:n.3958-226_3958-222delinsTAATG
ENST00000699604.1:c.*3788-226_*3788-222delinsTAATG	ENSP00000514472.1:n.*3788-226_*3788-222delinsTAATG
ENST00000699605.1:c.3538-226_3538-222delinsTAATG	ENSP00000514473.1:n.3538-226_3538-222delinsTAATG
ENST00000699606.1:n.2132-226_2132-222delinsTAATG
ENST00000685018.1:c.828-226_828-222delinsTAATG	ENSP00000510194.1:n.828-226_828-222delinsTAATG
ENST00000687278.1:c.1751-226_1751-222delinsTAATG	ENSP00000509593.1:n.1751-226_1751-222delinsTAATG
ENST00000689011.1:c.546-226_546-222delinsTAATG
ENST00000003084.11:c.3964-226_3964-222delinsTAATG MANE Select	ENSP00000003084.6:n.3964-226_3964-222delinsTAATG
ENST00000647720.1:c.1414-226_1414-222delinsTAATG
ENST00000649781.1:c.3781-226_3781-222delinsTAATG	ENSP00000497203.1:n.3781-226_3781-222delinsTAATG
ENST00000003084.10:c.3964-226_3964-222delinsTAATG	ENSP00000003084.6:n.3964-226_3964-222delinsTAATG
ENST00000426809.5:c.3874-226_3874-222delinsTAATG	ENSP00000389119.1:n.3874-226_3874-222delinsTAATG
ENST00000600166.1:c.90-226_90-222delinsTAATG
NM_000492.3:c.3964-226_3964-222delinsTAATG , LRG_663t1:c.3964-226_3964-222delinsTAATG	NP_000483.3:n.3964-226_3964-222delinsTAATG
XM_011515751.1:c.4054-226_4054-222delinsTAATG	XP_011514053.1:n.4054-226_4054-222delinsTAATG
XM_011515752.1:c.4054-226_4054-222delinsTAATG	XP_011514054.1:n.4054-226_4054-222delinsTAATG
XM_011515753.1:c.3721-226_3721-222delinsTAATG	XP_011514055.1:n.3721-226_3721-222delinsTAATG
XM_011515754.1:c.3721-226_3721-222delinsTAATG	XP_011514056.1:n.3721-226_3721-222delinsTAATG
NM_000492.4:c.3964-226_3964-222delinsTAATG MANE Select	NP_000483.3:n.3964-226_3964-222delinsTAATG