Canonical Allele Identifier: CA457227306

Gene: CFTR

Linked Data

• ClinVar Variation Id: 1153176
• ClinVar RCV Id: RCV001494760
• dbSNP Id: rs1232726281
• gnomAD v2: 7-117227876-T-C
• gnomAD v4: 7-117587822-T-C
• MyVariant Identifiers: chr7:g.117227876T>C (hg19) ; chr7:g.117587822T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117587822T>C , CM000669.2:g.117587822T>C	GRCh38
NC_000007.13:g.117227876T>C , CM000669.1:g.117227876T>C	GRCh37
NC_000007.12:g.117015112T>C	NCBI36
NG_016465.4:g.127039T>C , LRG_663:g.127039T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.1668T>C	ENSP00000497673.2:p.Ile556=
ENST00000647978.2:c.*1382T>C	ENSP00000497658.1:n.*1382T>C
ENST00000649781.2:c.1485T>C	ENSP00000497203.1:p.Ile495=
ENST00000685018.2:c.1668T>C	ENSP00000510194.2:p.Ile556=
ENST00000687278.2:c.1668T>C	ENSP00000509593.2:p.Ile556=
ENST00000699585.1:c.1668T>C	ENSP00000514456.1:p.Ile556=
ENST00000699598.1:c.1668T>C	ENSP00000514467.1:p.Ile556=
ENST00000699599.1:c.1668T>C	ENSP00000514468.1:p.Ile556=
ENST00000699600.1:c.1668T>C	ENSP00000514469.1:p.Ile556=
ENST00000699601.1:c.1668T>C	ENSP00000514470.1:p.Ile556=
ENST00000699602.1:c.1668T>C	ENSP00000514471.1:p.Ile556=
ENST00000699604.1:c.*1492T>C	ENSP00000514472.1:n.*1492T>C
ENST00000699605.1:c.1242T>C	ENSP00000514473.1:p.Ile414=
ENST00000003084.11:c.1668T>C MANE Select	ENSP00000003084.6:p.Ile556=
ENST00000647978.1:c.*1382T>C	ENSP00000497658.1:n.*1382T>C
ENST00000648260.1:c.1402-15004T>C	ENSP00000497957.1:n.1402-15004T>C
ENST00000649406.1:c.1485T>C	ENSP00000497965.1:p.Ile495=
ENST00000649781.1:c.1485T>C	ENSP00000497203.1:p.Ile495=
ENST00000003084.10:c.1668T>C	ENSP00000003084.6:p.Ile556=
ENST00000426809.5:c.1578T>C	ENSP00000389119.1:p.Ile526=
NM_000492.3:c.1668T>C , LRG_663t1:c.1668T>C	NP_000483.3:p.Ile556=
XM_011515751.1:c.1758T>C	XP_011514053.1:p.Ile586=
XM_011515752.1:c.1758T>C	XP_011514054.1:p.Ile586=
XM_011515753.1:c.1425T>C	XP_011514055.1:p.Ile475=
XM_011515754.1:c.1425T>C	XP_011514056.1:p.Ile475=
NM_000492.4:c.1668T>C MANE Select	NP_000483.3:p.Ile556=