Canonical Allele Identifier: CA368993711

Gene: CFTR

Linked Data

• ClinVar Variation Id: 2506208
• ClinVar RCV Id: RCV003236439
• gnomAD v4: 7-117614702-G-C
• MyVariant Identifiers: chr7:g.117254756G>C (hg19) ; chr7:g.117614702G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117614702G>C , CM000669.2:g.117614702G>C	GRCh38
NC_000007.13:g.117254756G>C , CM000669.1:g.117254756G>C	GRCh37
NC_000007.12:g.117041992G>C	NCBI36
NG_016465.4:g.153919G>C , LRG_663:g.153919G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3457G>C	ENSP00000497673.2:p.Val1153Leu
ENST00000647978.2:c.*3171G>C	ENSP00000497658.1:n.*3171G>C
ENST00000649781.2:c.3274G>C	ENSP00000497203.1:p.Val1092Leu
ENST00000685018.2:c.3457G>C	ENSP00000510194.2:p.Val1153Leu
ENST00000687278.2:c.3457G>C	ENSP00000509593.2:p.Val1153Leu
ENST00000699585.1:c.3457G>C	ENSP00000514456.1:p.Val1153Leu
ENST00000699598.1:c.3457G>C	ENSP00000514467.1:p.Val1153Leu
ENST00000699599.1:c.3457G>C	ENSP00000514468.1:p.Val1153Leu
ENST00000699600.1:c.3457G>C	ENSP00000514469.1:p.Val1153Leu
ENST00000699601.1:c.*1832G>C	ENSP00000514470.1:n.*1832G>C
ENST00000699602.1:c.3451G>C	ENSP00000514471.1:p.Val1151Leu
ENST00000699604.1:c.*3281G>C	ENSP00000514472.1:n.*3281G>C
ENST00000699605.1:c.3031G>C	ENSP00000514473.1:p.Val1011Leu
ENST00000685018.1:c.205G>C	ENSP00000510194.1:p.Val69Leu
ENST00000687278.1:c.1048G>C	ENSP00000509593.1:p.Val350Leu
ENST00000689011.1:c.39G>C
ENST00000003084.11:c.3457G>C MANE Select	ENSP00000003084.6:p.Val1153Leu
ENST00000647720.1:c.1107G>C
ENST00000648260.1:c.2239G>C	ENSP00000497957.1:p.Val747Leu
ENST00000649406.1:c.3274G>C	ENSP00000497965.1:p.Val1092Leu
ENST00000649781.1:c.3274G>C	ENSP00000497203.1:p.Val1092Leu
ENST00000003084.10:c.3457G>C	ENSP00000003084.6:p.Val1153Leu
ENST00000426809.5:c.3367G>C	ENSP00000389119.1:p.Val1123Leu
ENST00000468795.1:c.282G>C
NM_000492.3:c.3457G>C , LRG_663t1:c.3457G>C	NP_000483.3:p.Val1153Leu
XM_011515751.1:c.3547G>C	XP_011514053.1:p.Val1183Leu
XM_011515752.1:c.3547G>C	XP_011514054.1:p.Val1183Leu
XM_011515753.1:c.3214G>C	XP_011514055.1:p.Val1072Leu
XM_011515754.1:c.3214G>C	XP_011514056.1:p.Val1072Leu
NM_000492.4:c.3457G>C MANE Select	NP_000483.3:p.Val1153Leu