Canonical Allele Identifier: CA1737343357
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478734C= , CM000669.2:g.117478734C= GRCh38
NC_000007.13:g.117118788C= , CM000669.1:g.117118788C= GRCh37
NC_000007.12:g.116906024C= NCBI36
NG_016465.4:g.17951C= , LRG_663:g.17951C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-526+312C= ENSP00000417012.1:n.-526+312C=
ENST00000673785.1:c.-406+12903C= ENSP00000501235.1:n.-406+12903C=
ENST00000546407.1:n.166+2926C=
XM_011515751.1:c.41+312C= XP_011514053.1:n.41+312C=
XM_011515752.1:c.41+312C= XP_011514054.1:n.41+312C=
XM_011515754.1:c.-1363C= XP_011514056.1:n.-1363C=