Canonical Allele Identifier: CA1737343934
Gene: CFTR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117479476T= , CM000669.2:g.117479476T= GRCh38
NC_000007.13:g.117119530T= , CM000669.1:g.117119530T= GRCh37
NC_000007.12:g.116906766T= NCBI36
NG_016465.4:g.18693T= , LRG_663:g.18693T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000446805.2:c.-409T= ENSP00000417012.1:n.-409T=
ENST00000673785.1:c.-406+13645T= ENSP00000501235.1:n.-406+13645T=
ENST00000446805.1:c.-409T= ENSP00000417012.1:n.-409T=
ENST00000546407.1:n.166+3668T=
XM_011515751.1:c.143+131T= XP_011514053.1:n.143+131T=
XM_011515752.1:c.143+131T= XP_011514054.1:n.143+131T=
XM_011515753.1:c.-409T= XP_011514055.1:n.-409T=
XM_011515754.1:c.-737T= XP_011514056.1:n.-737T=
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