Canonical Allele Identifier: CA1737343618
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479015C= , CM000669.2:g.117479015C= GRCh38
NC_000007.13:g.117119069C= , CM000669.1:g.117119069C= GRCh37
NC_000007.12:g.116906305C= NCBI36
NG_016465.4:g.18232C= , LRG_663:g.18232C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-525-229C= ENSP00000417012.1:n.-525-229C=
ENST00000673785.1:c.-406+13184C= ENSP00000501235.1:n.-406+13184C=
ENST00000546407.1:n.166+3207C=
XM_011515751.1:c.42-229C= XP_011514053.1:n.42-229C=
XM_011515752.1:c.42-229C= XP_011514054.1:n.42-229C=
XM_011515754.1:c.-1082C= XP_011514056.1:n.-1082C=