Canonical Allele Identifier: CA1737343372
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117478749A= , CM000669.2:g.117478749A= GRCh38
NC_000007.13:g.117118803A= , CM000669.1:g.117118803A= GRCh37
NC_000007.12:g.116906039A= NCBI36
NG_016465.4:g.17966A= , LRG_663:g.17966A=

Transcript Alleles

HGVS Amino-acid change
ENST00000446805.2:c.-526+327A= ENSP00000417012.1:n.-526+327A=
ENST00000673785.1:c.-406+12918A= ENSP00000501235.1:n.-406+12918A=
ENST00000546407.1:n.166+2941A=
XM_011515751.1:c.41+327A= XP_011514053.1:n.41+327A=
XM_011515752.1:c.41+327A= XP_011514054.1:n.41+327A=
XM_011515754.1:c.-1348A= XP_011514056.1:n.-1348A=