Canonical Allele Identifier: CA368992122

Gene: CFTR

Linked Data

• gnomAD v4: 7-117611658-T-G
• MyVariant Identifiers: chr7:g.117251712T>G (hg19) ; chr7:g.117611658T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611658T>G , CM000669.2:g.117611658T>G	GRCh38
NC_000007.13:g.117251712T>G , CM000669.1:g.117251712T>G	GRCh37
NC_000007.12:g.117038948T>G	NCBI36
NG_016465.4:g.150875T>G , LRG_663:g.150875T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3217T>G	ENSP00000497673.2:p.Tyr1073Asp
ENST00000647978.2:c.*2931T>G	ENSP00000497658.1:n.*2931T>G
ENST00000649781.2:c.3034T>G	ENSP00000497203.1:p.Tyr1012Asp
ENST00000685018.2:c.3217T>G	ENSP00000510194.2:p.Tyr1073Asp
ENST00000687278.2:c.3217T>G	ENSP00000509593.2:p.Tyr1073Asp
ENST00000699585.1:c.3217T>G	ENSP00000514456.1:p.Tyr1073Asp
ENST00000699598.1:c.3217T>G	ENSP00000514467.1:p.Tyr1073Asp
ENST00000699599.1:c.3217T>G	ENSP00000514468.1:p.Tyr1073Asp
ENST00000699600.1:c.3217T>G	ENSP00000514469.1:p.Tyr1073Asp
ENST00000699601.1:c.*1517T>G	ENSP00000514470.1:n.*1517T>G
ENST00000699602.1:c.3217T>G	ENSP00000514471.1:p.Tyr1073Asp
ENST00000699604.1:c.*3041T>G	ENSP00000514472.1:n.*3041T>G
ENST00000699605.1:c.2791T>G	ENSP00000514473.1:p.Tyr931Asp
ENST00000687278.1:c.808T>G	ENSP00000509593.1:p.Tyr270Asp
ENST00000003084.11:c.3217T>G MANE Select	ENSP00000003084.6:p.Tyr1073Asp
ENST00000647720.1:c.867T>G
ENST00000648260.1:c.1999T>G	ENSP00000497957.1:p.Tyr667Asp
ENST00000649406.1:c.3034T>G	ENSP00000497965.1:p.Tyr1012Asp
ENST00000649781.1:c.3034T>G	ENSP00000497203.1:p.Tyr1012Asp
ENST00000003084.10:c.3217T>G	ENSP00000003084.6:p.Tyr1073Asp
ENST00000426809.5:c.3127T>G	ENSP00000389119.1:p.Tyr1043Asp
ENST00000468795.1:c.42T>G
NM_000492.3:c.3217T>G , LRG_663t1:c.3217T>G	NP_000483.3:p.Tyr1073Asp
XM_011515751.1:c.3307T>G	XP_011514053.1:p.Tyr1103Asp
XM_011515752.1:c.3307T>G	XP_011514054.1:p.Tyr1103Asp
XM_011515753.1:c.2974T>G	XP_011514055.1:p.Tyr992Asp
XM_011515754.1:c.2974T>G	XP_011514056.1:p.Tyr992Asp
NM_000492.4:c.3217T>G MANE Select	NP_000483.3:p.Tyr1073Asp