Canonical Allele Identifier: CA2777590974
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479488G>C , CM000669.2:g.117479488G>C GRCh38
NC_000007.13:g.117119542G>C , CM000669.1:g.117119542G>C GRCh37
NC_000007.12:g.116906778G>C NCBI36
NG_016465.4:g.18705G>C , LRG_663:g.18705G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-397G>C ENSP00000417012.1:n.-397G>C
ENST00000673785.1:c.-406+13657G>C ENSP00000501235.1:n.-406+13657G>C
ENST00000446805.1:c.-397G>C ENSP00000417012.1:n.-397G>C
ENST00000546407.1:n.166+3680G>C
XM_011515751.1:c.143+143G>C XP_011514053.1:n.143+143G>C
XM_011515752.1:c.143+143G>C XP_011514054.1:n.143+143G>C
XM_011515753.1:c.-397G>C XP_011514055.1:n.-397G>C
XM_011515754.1:c.-725G>C XP_011514056.1:n.-725G>C