Canonical Allele Identifier: CA2695208296

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117531075del , CM000669.2:g.117531075del	GRCh38
NC_000007.13:g.117171129del , CM000669.1:g.117171129del	GRCh37
NC_000007.12:g.116958365del	NCBI36
NG_016465.4:g.70292del , LRG_663:g.70292del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.450del	ENSP00000497673.2:p.Met150IlefsTer3
ENST00000647978.2:c.*347del	ENSP00000497658.1:n.*347del
ENST00000649781.2:c.450del	ENSP00000497203.1:p.Met150IlefsTer3
ENST00000685018.2:c.450del	ENSP00000510194.2:p.Met150IlefsTer3
ENST00000687278.2:c.450del	ENSP00000509593.2:p.Met150IlefsTer3
ENST00000699585.1:c.450del	ENSP00000514456.1:p.Met150IlefsTer3
ENST00000699596.1:c.450del	ENSP00000514465.1:p.Met150IlefsTer3
ENST00000699597.1:c.450del	ENSP00000514466.1:p.Met150IlefsTer3
ENST00000699598.1:c.450del	ENSP00000514467.1:p.Met150IlefsTer3
ENST00000699599.1:c.450del	ENSP00000514468.1:p.Met150IlefsTer3
ENST00000699600.1:c.450del	ENSP00000514469.1:p.Met150IlefsTer3
ENST00000699601.1:c.450del	ENSP00000514470.1:p.Met150IlefsTer3
ENST00000699602.1:c.450del	ENSP00000514471.1:p.Met150IlefsTer3
ENST00000699604.1:c.*274del	ENSP00000514472.1:n.*274del
ENST00000699605.1:c.207del	ENSP00000514473.1:p.Met69IlefsTer3
ENST00000003084.11:c.450del MANE Select	ENSP00000003084.6:p.Met150IlefsTer3
ENST00000647978.1:c.*347del	ENSP00000497658.1:n.*347del
ENST00000648260.1:c.450del	ENSP00000497957.1:p.Met150IlefsTer3
ENST00000649406.1:c.450del	ENSP00000497965.1:p.Met150IlefsTer3
ENST00000649781.1:c.450del	ENSP00000497203.1:p.Met150IlefsTer3
ENST00000673785.1:c.207del	ENSP00000501235.1:p.Met69IlefsTer3
ENST00000003084.10:c.450del	ENSP00000003084.6:p.Met150IlefsTer3
ENST00000426809.5:c.450del	ENSP00000389119.1:p.Met150IlefsTer3
NM_000492.3:c.450del , LRG_663t1:c.450del	NP_000483.3:p.Met150IlefsTer3
XM_011515751.1:c.540del	XP_011514053.1:p.Met180IlefsTer3
XM_011515752.1:c.540del	XP_011514054.1:p.Met180IlefsTer3
XM_011515753.1:c.207del	XP_011514055.1:p.Met69IlefsTer3
XM_011515754.1:c.207del	XP_011514056.1:p.Met69IlefsTer3
NM_000492.4:c.450del MANE Select	NP_000483.3:p.Met150IlefsTer3