Canonical Allele Identifier: CA1737344066
Gene: CFTR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479616T= , CM000669.2:g.117479616T= GRCh38
NC_000007.13:g.117119670T= , CM000669.1:g.117119670T= GRCh37
NC_000007.12:g.116906906T= NCBI36
NG_016465.4:g.18833T= , LRG_663:g.18833T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-269T= ENSP00000417012.1:n.-269T=
ENST00000673785.1:c.-406+13785T= ENSP00000501235.1:n.-406+13785T=
ENST00000446805.1:c.-269T= ENSP00000417012.1:n.-269T=
ENST00000546407.1:n.166+3808T=
XM_011515751.1:c.143+271T= XP_011514053.1:n.143+271T=
XM_011515752.1:c.143+271T= XP_011514054.1:n.143+271T=
XM_011515753.1:c.-269T= XP_011514055.1:n.-269T=
XM_011515754.1:c.-597T= XP_011514056.1:n.-597T=
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