Canonical Allele Identifier: CA368989109

Gene: CFTR

Linked Data

• ClinVar Variation Id: 1798061
• ClinVar RCV Id: RCV002441875
• gnomAD v4: 7-117606716-A-T
• MyVariant Identifiers: chr7:g.117246770A>T (hg19) ; chr7:g.117606716A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117606716A>T , CM000669.2:g.117606716A>T	GRCh38
NC_000007.13:g.117246770A>T , CM000669.1:g.117246770A>T	GRCh37
NC_000007.12:g.117034006A>T	NCBI36
NG_016465.4:g.145933A>T , LRG_663:g.145933A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2951A>T	ENSP00000497673.2:p.Asp984Val
ENST00000647978.2:c.*2665A>T	ENSP00000497658.1:n.*2665A>T
ENST00000649781.2:c.2768A>T	ENSP00000497203.1:p.Asp923Val
ENST00000685018.2:c.2951A>T	ENSP00000510194.2:p.Asp984Val
ENST00000687278.2:c.2951A>T	ENSP00000509593.2:p.Asp984Val
ENST00000699585.1:c.2951A>T	ENSP00000514456.1:p.Asp984Val
ENST00000699598.1:c.2951A>T	ENSP00000514467.1:p.Asp984Val
ENST00000699599.1:c.2951A>T	ENSP00000514468.1:p.Asp984Val
ENST00000699600.1:c.2951A>T	ENSP00000514469.1:p.Asp984Val
ENST00000699601.1:c.*1251A>T	ENSP00000514470.1:n.*1251A>T
ENST00000699602.1:c.2951A>T	ENSP00000514471.1:p.Asp984Val
ENST00000699604.1:c.*2775A>T	ENSP00000514472.1:n.*2775A>T
ENST00000699605.1:c.2525A>T	ENSP00000514473.1:p.Asp842Val
ENST00000687278.1:c.542A>T	ENSP00000509593.1:p.Asp181Val
ENST00000003084.11:c.2951A>T MANE Select	ENSP00000003084.6:p.Asp984Val
ENST00000647720.1:c.601A>T
ENST00000648260.1:c.1733A>T	ENSP00000497957.1:p.Asp578Val
ENST00000649406.1:c.2768A>T	ENSP00000497965.1:p.Asp923Val
ENST00000649781.1:c.2768A>T	ENSP00000497203.1:p.Asp923Val
ENST00000003084.10:c.2951A>T	ENSP00000003084.6:p.Asp984Val
ENST00000426809.5:c.2861A>T	ENSP00000389119.1:p.Asp954Val
NM_000492.3:c.2951A>T , LRG_663t1:c.2951A>T	NP_000483.3:p.Asp984Val
XM_011515751.1:c.3041A>T	XP_011514053.1:p.Asp1014Val
XM_011515752.1:c.3041A>T	XP_011514054.1:p.Asp1014Val
XM_011515753.1:c.2708A>T	XP_011514055.1:p.Asp903Val
XM_011515754.1:c.2708A>T	XP_011514056.1:p.Asp903Val
NM_000492.4:c.2951A>T MANE Select	NP_000483.3:p.Asp984Val