Canonical Allele Identifier: CA1737343755
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479267C= , CM000669.2:g.117479267C= GRCh38
NC_000007.13:g.117119321C= , CM000669.1:g.117119321C= GRCh37
NC_000007.12:g.116906557C= NCBI36
NG_016465.4:g.18484C= , LRG_663:g.18484C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-502C= ENSP00000417012.1:n.-502C=
ENST00000673785.1:c.-406+13436C= ENSP00000501235.1:n.-406+13436C=
ENST00000546407.1:n.166+3459C=
XM_011515751.1:c.65C= XP_011514053.1:p.Pro22=
XM_011515752.1:c.65C= XP_011514054.1:p.Pro22=
XM_011515754.1:c.-830C= XP_011514056.1:n.-830C=