Canonical Allele Identifier: CA457230034

Gene: CFTR

Linked Data

• ClinVar Variation Id: 1114599
• ClinVar RCV Id: RCV001442370
• dbSNP Id: rs2116084700
• MyVariant Identifiers: chr7:g.117251732C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611678C>T , CM000669.2:g.117611678C>T	GRCh38
NC_000007.13:g.117251732C>T , CM000669.1:g.117251732C>T	GRCh37
NC_000007.12:g.117038968C>T	NCBI36
NG_016465.4:g.150895C>T , LRG_663:g.150895C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3237C>T	ENSP00000497673.2:p.His1079=
ENST00000647978.2:c.*2951C>T	ENSP00000497658.1:n.*2951C>T
ENST00000649781.2:c.3054C>T	ENSP00000497203.1:p.His1018=
ENST00000685018.2:c.3237C>T	ENSP00000510194.2:p.His1079=
ENST00000687278.2:c.3237C>T	ENSP00000509593.2:p.His1079=
ENST00000699585.1:c.3237C>T	ENSP00000514456.1:p.His1079=
ENST00000699598.1:c.3237C>T	ENSP00000514467.1:p.His1079=
ENST00000699599.1:c.3237C>T	ENSP00000514468.1:p.His1079=
ENST00000699600.1:c.3237C>T	ENSP00000514469.1:p.His1079=
ENST00000699601.1:c.*1537C>T	ENSP00000514470.1:n.*1537C>T
ENST00000699602.1:c.3237C>T	ENSP00000514471.1:p.His1079=
ENST00000699604.1:c.*3061C>T	ENSP00000514472.1:n.*3061C>T
ENST00000699605.1:c.2811C>T	ENSP00000514473.1:p.His937=
ENST00000687278.1:c.828C>T	ENSP00000509593.1:p.His276=
ENST00000003084.11:c.3237C>T MANE Select	ENSP00000003084.6:p.His1079=
ENST00000647720.1:c.887C>T
ENST00000648260.1:c.2019C>T	ENSP00000497957.1:p.His673=
ENST00000649406.1:c.3054C>T	ENSP00000497965.1:p.His1018=
ENST00000649781.1:c.3054C>T	ENSP00000497203.1:p.His1018=
ENST00000003084.10:c.3237C>T	ENSP00000003084.6:p.His1079=
ENST00000426809.5:c.3147C>T	ENSP00000389119.1:p.His1049=
ENST00000468795.1:c.62C>T
NM_000492.3:c.3237C>T , LRG_663t1:c.3237C>T	NP_000483.3:p.His1079=
XM_011515751.1:c.3327C>T	XP_011514053.1:p.His1109=
XM_011515752.1:c.3327C>T	XP_011514054.1:p.His1109=
XM_011515753.1:c.2994C>T	XP_011514055.1:p.His998=
XM_011515754.1:c.2994C>T	XP_011514056.1:p.His998=
NM_000492.4:c.3237C>T MANE Select	NP_000483.3:p.His1079=