Canonical Allele Identifier: CA1737344060
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479611T= , CM000669.2:g.117479611T= GRCh38
NC_000007.13:g.117119665T= , CM000669.1:g.117119665T= GRCh37
NC_000007.12:g.116906901T= NCBI36
NG_016465.4:g.18828T= , LRG_663:g.18828T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-274T= ENSP00000417012.1:n.-274T=
ENST00000673785.1:c.-406+13780T= ENSP00000501235.1:n.-406+13780T=
ENST00000446805.1:c.-274T= ENSP00000417012.1:n.-274T=
ENST00000546407.1:n.166+3803T=
XM_011515751.1:c.143+266T= XP_011514053.1:n.143+266T=
XM_011515752.1:c.143+266T= XP_011514054.1:n.143+266T=
XM_011515753.1:c.-274T= XP_011514055.1:n.-274T=
XM_011515754.1:c.-602T= XP_011514056.1:n.-602T=