Canonical Allele Identifier: CA368991925

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117251667A>T (hg19) ; chr7:g.117611613A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611613A>T , CM000669.2:g.117611613A>T	GRCh38
NC_000007.13:g.117251667A>T , CM000669.1:g.117251667A>T	GRCh37
NC_000007.12:g.117038903A>T	NCBI36
NG_016465.4:g.150830A>T , LRG_663:g.150830A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3172A>T	ENSP00000497673.2:p.Ser1058Cys
ENST00000647978.2:c.*2886A>T	ENSP00000497658.1:n.*2886A>T
ENST00000649781.2:c.2989A>T	ENSP00000497203.1:p.Ser997Cys
ENST00000685018.2:c.3172A>T	ENSP00000510194.2:p.Ser1058Cys
ENST00000687278.2:c.3172A>T	ENSP00000509593.2:p.Ser1058Cys
ENST00000699585.1:c.3172A>T	ENSP00000514456.1:p.Ser1058Cys
ENST00000699598.1:c.3172A>T	ENSP00000514467.1:p.Ser1058Cys
ENST00000699599.1:c.3172A>T	ENSP00000514468.1:p.Ser1058Cys
ENST00000699600.1:c.3172A>T	ENSP00000514469.1:p.Ser1058Cys
ENST00000699601.1:c.*1472A>T	ENSP00000514470.1:n.*1472A>T
ENST00000699602.1:c.3172A>T	ENSP00000514471.1:p.Ser1058Cys
ENST00000699604.1:c.*2996A>T	ENSP00000514472.1:n.*2996A>T
ENST00000699605.1:c.2746A>T	ENSP00000514473.1:p.Ser916Cys
ENST00000687278.1:c.763A>T	ENSP00000509593.1:p.Ser255Cys
ENST00000003084.11:c.3172A>T MANE Select	ENSP00000003084.6:p.Ser1058Cys
ENST00000647720.1:c.822A>T
ENST00000648260.1:c.1954A>T	ENSP00000497957.1:p.Ser652Cys
ENST00000649406.1:c.2989A>T	ENSP00000497965.1:p.Ser997Cys
ENST00000649781.1:c.2989A>T	ENSP00000497203.1:p.Ser997Cys
ENST00000003084.10:c.3172A>T	ENSP00000003084.6:p.Ser1058Cys
ENST00000426809.5:c.3082A>T	ENSP00000389119.1:p.Ser1028Cys
NM_000492.3:c.3172A>T , LRG_663t1:c.3172A>T	NP_000483.3:p.Ser1058Cys
XM_011515751.1:c.3262A>T	XP_011514053.1:p.Ser1088Cys
XM_011515752.1:c.3262A>T	XP_011514054.1:p.Ser1088Cys
XM_011515753.1:c.2929A>T	XP_011514055.1:p.Ser977Cys
XM_011515754.1:c.2929A>T	XP_011514056.1:p.Ser977Cys
NM_000492.4:c.3172A>T MANE Select	NP_000483.3:p.Ser1058Cys