Canonical Allele Identifier: CA1737331708
Gene: CFTR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.117540066A= , CM000669.2:g.117540066A= GRCh38
NC_000007.13:g.117180120A= , CM000669.1:g.117180120A= GRCh37
NC_000007.12:g.116967356A= NCBI36
NG_016465.4:g.79283A= , LRG_663:g.79283A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647720.2:c.870-34A= ENSP00000497673.2:n.870-34A=
ENST00000647978.2:c.*767-34A= ENSP00000497658.1:n.*767-34A=
ENST00000649781.2:c.870-34A= ENSP00000497203.1:n.870-34A=
ENST00000685018.2:c.870-34A= ENSP00000510194.2:n.870-34A=
ENST00000687278.2:c.870-34A= ENSP00000509593.2:n.870-34A=
ENST00000699585.1:c.870-34A= ENSP00000514456.1:n.870-34A=
ENST00000699596.1:c.870-34A= ENSP00000514465.1:n.870-34A=
ENST00000699597.1:c.870-34A= ENSP00000514466.1:n.870-34A=
ENST00000699598.1:c.870-34A= ENSP00000514467.1:n.870-34A=
ENST00000699599.1:c.870-34A= ENSP00000514468.1:n.870-34A=
ENST00000699600.1:c.870-34A= ENSP00000514469.1:n.870-34A=
ENST00000699601.1:c.870-34A= ENSP00000514470.1:n.870-34A=
ENST00000699602.1:c.870-34A= ENSP00000514471.1:n.870-34A=
ENST00000699604.1:c.*694-34A= ENSP00000514472.1:n.*694-34A=
ENST00000699605.1:c.627-34A= ENSP00000514473.1:n.627-34A=
ENST00000003084.11:c.870-34A= MANE Select ENSP00000003084.6:n.870-34A=
ENST00000647978.1:c.*767-34A= ENSP00000497658.1:n.*767-34A=
ENST00000648260.1:c.870-34A= ENSP00000497957.1:n.870-34A=
ENST00000649406.1:c.870-34A= ENSP00000497965.1:n.870-34A=
ENST00000649781.1:c.870-34A= ENSP00000497203.1:n.870-34A=
ENST00000673785.1:c.627-34A= ENSP00000501235.1:n.627-34A=
ENST00000003084.10:c.870-34A= ENSP00000003084.6:n.870-34A=
ENST00000426809.5:c.780-34A= ENSP00000389119.1:n.780-34A=
NM_000492.3:c.870-34A= , LRG_663t1:c.870-34A= NP_000483.3:n.870-34A=
XM_011515751.1:c.960-34A= XP_011514053.1:n.960-34A=
XM_011515752.1:c.960-34A= XP_011514054.1:n.960-34A=
XM_011515753.1:c.627-34A= XP_011514055.1:n.627-34A=
XM_011515754.1:c.627-34A= XP_011514056.1:n.627-34A=
NM_000492.4:c.870-34A= MANE Select NP_000483.3:n.870-34A=