Canonical Allele Identifier: CA457229982

Gene: CFTR

Linked Data

• COSMIC: COSM484673
• MyVariant Identifiers: chr7:g.117251654T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611600T>G , CM000669.2:g.117611600T>G	GRCh38
NC_000007.13:g.117251654T>G , CM000669.1:g.117251654T>G	GRCh37
NC_000007.12:g.117038890T>G	NCBI36
NG_016465.4:g.150817T>G , LRG_663:g.150817T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3159T>G	ENSP00000497673.2:p.Thr1053=
ENST00000647978.2:c.*2873T>G	ENSP00000497658.1:n.*2873T>G
ENST00000649781.2:c.2976T>G	ENSP00000497203.1:p.Thr992=
ENST00000685018.2:c.3159T>G	ENSP00000510194.2:p.Thr1053=
ENST00000687278.2:c.3159T>G	ENSP00000509593.2:p.Thr1053=
ENST00000699585.1:c.3159T>G	ENSP00000514456.1:p.Thr1053=
ENST00000699598.1:c.3159T>G	ENSP00000514467.1:p.Thr1053=
ENST00000699599.1:c.3159T>G	ENSP00000514468.1:p.Thr1053=
ENST00000699600.1:c.3159T>G	ENSP00000514469.1:p.Thr1053=
ENST00000699601.1:c.*1459T>G	ENSP00000514470.1:n.*1459T>G
ENST00000699602.1:c.3159T>G	ENSP00000514471.1:p.Thr1053=
ENST00000699604.1:c.*2983T>G	ENSP00000514472.1:n.*2983T>G
ENST00000699605.1:c.2733T>G	ENSP00000514473.1:p.Thr911=
ENST00000687278.1:c.750T>G	ENSP00000509593.1:p.Thr250=
ENST00000003084.11:c.3159T>G MANE Select	ENSP00000003084.6:p.Thr1053=
ENST00000647720.1:c.809T>G
ENST00000648260.1:c.1941T>G	ENSP00000497957.1:p.Thr647=
ENST00000649406.1:c.2976T>G	ENSP00000497965.1:p.Thr992=
ENST00000649781.1:c.2976T>G	ENSP00000497203.1:p.Thr992=
ENST00000003084.10:c.3159T>G	ENSP00000003084.6:p.Thr1053=
ENST00000426809.5:c.3069T>G	ENSP00000389119.1:p.Thr1023=
NM_000492.3:c.3159T>G , LRG_663t1:c.3159T>G	NP_000483.3:p.Thr1053=
XM_011515751.1:c.3249T>G	XP_011514053.1:p.Thr1083=
XM_011515752.1:c.3249T>G	XP_011514054.1:p.Thr1083=
XM_011515753.1:c.2916T>G	XP_011514055.1:p.Thr972=
XM_011515754.1:c.2916T>G	XP_011514056.1:p.Thr972=
NM_000492.4:c.3159T>G MANE Select	NP_000483.3:p.Thr1053=