Canonical Allele Identifier: CA457448592
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1086609
ClinVar RCV Id: RCV001404420
dbSNP Id: rs2116683646
MyVariant Identifiers: chr7:g.117180190G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117540136G>C , CM000669.2:g.117540136G>C GRCh38
NC_000007.13:g.117180190G>C , CM000669.1:g.117180190G>C GRCh37
NC_000007.12:g.116967426G>C NCBI36
NG_016465.4:g.79353G>C , LRG_663:g.79353G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.906G>C ENSP00000497673.2:p.Val302=
ENST00000647978.2:c.*803G>C ENSP00000497658.1:n.*803G>C
ENST00000649781.2:c.906G>C ENSP00000497203.1:p.Val302=
ENST00000685018.2:c.906G>C ENSP00000510194.2:p.Val302=
ENST00000687278.2:c.906G>C ENSP00000509593.2:p.Val302=
ENST00000699585.1:c.906G>C ENSP00000514456.1:p.Val302=
ENST00000699596.1:c.906G>C ENSP00000514465.1:p.Val302=
ENST00000699597.1:c.906G>C ENSP00000514466.1:p.Val302=
ENST00000699598.1:c.906G>C ENSP00000514467.1:p.Val302=
ENST00000699599.1:c.906G>C ENSP00000514468.1:p.Val302=
ENST00000699600.1:c.906G>C ENSP00000514469.1:p.Val302=
ENST00000699601.1:c.906G>C ENSP00000514470.1:p.Val302=
ENST00000699602.1:c.906G>C ENSP00000514471.1:p.Val302=
ENST00000699604.1:c.*730G>C ENSP00000514472.1:n.*730G>C
ENST00000699605.1:c.663G>C ENSP00000514473.1:p.Val221=
ENST00000003084.11:c.906G>C MANE Select ENSP00000003084.6:p.Val302=
ENST00000647978.1:c.*803G>C ENSP00000497658.1:n.*803G>C
ENST00000648260.1:c.906G>C ENSP00000497957.1:p.Val302=
ENST00000649406.1:c.906G>C ENSP00000497965.1:p.Val302=
ENST00000649781.1:c.906G>C ENSP00000497203.1:p.Val302=
ENST00000673785.1:c.663G>C ENSP00000501235.1:p.Val221=
ENST00000003084.10:c.906G>C ENSP00000003084.6:p.Val302=
ENST00000426809.5:c.816G>C ENSP00000389119.1:p.Val272=
NM_000492.3:c.906G>C , LRG_663t1:c.906G>C NP_000483.3:p.Val302=
XM_011515751.1:c.996G>C XP_011514053.1:p.Val332=
XM_011515752.1:c.996G>C XP_011514054.1:p.Val332=
XM_011515753.1:c.663G>C XP_011514055.1:p.Val221=
XM_011515754.1:c.663G>C XP_011514056.1:p.Val221=
NM_000492.4:c.906G>C MANE Select NP_000483.3:p.Val302=