Canonical Allele Identifier: CA16041142

Gene: CFTR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117666937C>G , CM000669.2:g.117666937C>G	GRCh38
NC_000007.13:g.117306991C>G , CM000669.1:g.117306991C>G	GRCh37
NC_000007.12:g.117094227C>G	NCBI36
NG_016465.4:g.206154C>G , LRG_663:g.206154C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000492.4:c.4272C>G MANE Select	NP_000483.3:p.Tyr1424Ter
ENST00000003084.11:c.4272C>G MANE Select	ENSP00000003084.6:p.Tyr1424Ter
NM_000492.3:c.4272C>G , LRG_663t1:c.4272C>G	NP_000483.3:p.Tyr1424Ter
ENST00000003084.10:c.4272C>G	ENSP00000003084.6:p.Tyr1424Ter
ENST00000426809.5:c.4182C>G	ENSP00000389119.1:p.Tyr1394Ter
ENST00000600166.1:c.368+1373C>G
ENST00000647720.1:c.1722C>G
ENST00000647720.2:c.*481C>G	ENSP00000497673.2:n.*481C>G
ENST00000647978.2:c.*3986C>G	ENSP00000497658.1:n.*3986C>G
ENST00000649781.1:c.4089C>G	ENSP00000497203.1:p.Tyr1363Ter
ENST00000649781.2:c.4089C>G	ENSP00000497203.1:p.Tyr1363Ter
ENST00000685018.1:c.1136C>G	ENSP00000510194.1:n.1136C>G
ENST00000685018.2:c.*485C>G	ENSP00000510194.2:n.*485C>G
ENST00000687278.1:c.2030-665C>G	ENSP00000509593.1:n.2030-665C>G
ENST00000687278.2:c.*896-665C>G	ENSP00000509593.2:n.*896-665C>G
ENST00000689011.1:c.1114C>G
ENST00000699585.1:c.*741C>G	ENSP00000514456.1:n.*741C>G
ENST00000699598.1:c.4265C>G	ENSP00000514467.1:p.Thr1422Arg
ENST00000699599.1:c.*485C>G	ENSP00000514468.1:n.*485C>G
ENST00000699600.1:c.*904-665C>G	ENSP00000514469.1:n.*904-665C>G
ENST00000699601.1:c.*2647C>G	ENSP00000514470.1:n.*2647C>G
ENST00000699602.1:c.4266C>G	ENSP00000514471.1:p.Tyr1422Ter
ENST00000699604.1:c.*4096C>G	ENSP00000514472.1:n.*4096C>G
ENST00000699605.1:c.3846C>G	ENSP00000514473.1:p.Tyr1282Ter
ENST00000699606.1:n.3783C>G
XM_011515751.1:c.4362C>G	XP_011514053.1:p.Tyr1454Ter
XM_011515753.1:c.4029C>G	XP_011514055.1:p.Tyr1343Ter
XM_011515754.1:c.4029C>G	XP_011514056.1:p.Tyr1343Ter