Canonical Allele Identifier: CA1737385537

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117610758_117610761delinsTCTG , CM000669.2:g.117610758_117610761delinsTCTG	GRCh38
NC_000007.13:g.117250812_117250815delinsTCTG , CM000669.1:g.117250812_117250815delinsTCTG	GRCh37
NC_000007.12:g.117038048_117038051delinsTCTG	NCBI36
NG_016465.4:g.149975_149978delinsTCTG , LRG_663:g.149975_149978delinsTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3139+89_3139+92delinsTCTG	ENSP00000497673.2:n.3139+89_3139+92delinsTCTG
ENST00000647978.2:c.*2853+89_*2853+92delinsTCTG	ENSP00000497658.1:n.*2853+89_*2853+92delinsTCTG
ENST00000649781.2:c.2956+89_2956+92delinsTCTG	ENSP00000497203.1:n.2956+89_2956+92delinsTCTG
ENST00000685018.2:c.3139+89_3139+92delinsTCTG	ENSP00000510194.2:n.3139+89_3139+92delinsTCTG
ENST00000687278.2:c.3139+89_3139+92delinsTCTG	ENSP00000509593.2:n.3139+89_3139+92delinsTCTG
ENST00000699585.1:c.3139+89_3139+92delinsTCTG	ENSP00000514456.1:n.3139+89_3139+92delinsTCTG
ENST00000699598.1:c.3139+89_3139+92delinsTCTG	ENSP00000514467.1:n.3139+89_3139+92delinsTCTG
ENST00000699599.1:c.3139+89_3139+92delinsTCTG	ENSP00000514468.1:n.3139+89_3139+92delinsTCTG
ENST00000699600.1:c.3139+89_3139+92delinsTCTG	ENSP00000514469.1:n.3139+89_3139+92delinsTCTG
ENST00000699601.1:c.*1439+89_*1439+92delinsTCTG	ENSP00000514470.1:n.*1439+89_*1439+92delinsTCTG
ENST00000699602.1:c.3139+89_3139+92delinsTCTG	ENSP00000514471.1:n.3139+89_3139+92delinsTCTG
ENST00000699604.1:c.*2963+89_*2963+92delinsTCTG	ENSP00000514472.1:n.*2963+89_*2963+92delinsTCTG
ENST00000699605.1:c.2713+89_2713+92delinsTCTG	ENSP00000514473.1:n.2713+89_2713+92delinsTCTG
ENST00000687278.1:c.730+89_730+92delinsTCTG	ENSP00000509593.1:n.730+89_730+92delinsTCTG
ENST00000003084.11:c.3139+89_3139+92delinsTCTG MANE Select	ENSP00000003084.6:n.3139+89_3139+92delinsTCTG
ENST00000647720.1:c.789+89_789+92delinsTCTG
ENST00000648260.1:c.1921+89_1921+92delinsTCTG	ENSP00000497957.1:n.1921+89_1921+92delinsTCTG
ENST00000649406.1:c.2956+89_2956+92delinsTCTG	ENSP00000497965.1:n.2956+89_2956+92delinsTCTG
ENST00000649781.1:c.2956+89_2956+92delinsTCTG	ENSP00000497203.1:n.2956+89_2956+92delinsTCTG
ENST00000003084.10:c.3139+89_3139+92delinsTCTG	ENSP00000003084.6:n.3139+89_3139+92delinsTCTG
ENST00000426809.5:c.3049+89_3049+92delinsTCTG	ENSP00000389119.1:n.3049+89_3049+92delinsTCTG
NM_000492.3:c.3139+89_3139+92delinsTCTG , LRG_663t1:c.3139+89_3139+92delinsTCTG	NP_000483.3:n.3139+89_3139+92delinsTCTG
XM_011515751.1:c.3229+89_3229+92delinsTCTG	XP_011514053.1:n.3229+89_3229+92delinsTCTG
XM_011515752.1:c.3229+89_3229+92delinsTCTG	XP_011514054.1:n.3229+89_3229+92delinsTCTG
XM_011515753.1:c.2896+89_2896+92delinsTCTG	XP_011514055.1:n.2896+89_2896+92delinsTCTG
XM_011515754.1:c.2896+89_2896+92delinsTCTG	XP_011514056.1:n.2896+89_2896+92delinsTCTG
NM_000492.4:c.3139+89_3139+92delinsTCTG MANE Select	NP_000483.3:n.3139+89_3139+92delinsTCTG