Canonical Allele Identifier: CA1737344003
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479557C= , CM000669.2:g.117479557C= GRCh38
NC_000007.13:g.117119611C= , CM000669.1:g.117119611C= GRCh37
NC_000007.12:g.116906847C= NCBI36
NG_016465.4:g.18774C= , LRG_663:g.18774C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-328C= ENSP00000417012.1:n.-328C=
ENST00000673785.1:c.-406+13726C= ENSP00000501235.1:n.-406+13726C=
ENST00000446805.1:c.-328C= ENSP00000417012.1:n.-328C=
ENST00000546407.1:n.166+3749C=
XM_011515751.1:c.143+212C= XP_011514053.1:n.143+212C=
XM_011515752.1:c.143+212C= XP_011514054.1:n.143+212C=
XM_011515753.1:c.-328C= XP_011514055.1:n.-328C=
XM_011515754.1:c.-656C= XP_011514056.1:n.-656C=