Canonical Allele Identifier: CA2740097511
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 3054540
ClinVar RCV Id: RCV004540796
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479592G>A , CM000669.2:g.117479592G>A GRCh38
NC_000007.13:g.117119646G>A , CM000669.1:g.117119646G>A GRCh37
NC_000007.12:g.116906882G>A NCBI36
NG_016465.4:g.18809G>A , LRG_663:g.18809G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-293G>A ENSP00000417012.1:n.-293G>A
ENST00000673785.1:c.-406+13761G>A ENSP00000501235.1:n.-406+13761G>A
ENST00000446805.1:c.-293G>A ENSP00000417012.1:n.-293G>A
ENST00000546407.1:n.166+3784G>A
XM_011515751.1:c.143+247G>A XP_011514053.1:n.143+247G>A
XM_011515752.1:c.143+247G>A XP_011514054.1:n.143+247G>A
XM_011515753.1:c.-293G>A XP_011514055.1:n.-293G>A
XM_011515754.1:c.-621G>A XP_011514056.1:n.-621G>A
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