Canonical Allele Identifier: CA913111906

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117144418dup (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117504364dup , CM000669.2:g.117504364dup	GRCh38
NC_000007.13:g.117144418dup , CM000669.1:g.117144418dup	GRCh37
NC_000007.12:g.116931654dup	NCBI36
NG_016465.4:g.43581dup , LRG_663:g.43581dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.164+1dup
ENST00000647978.2:c.164+1dup
ENST00000649781.2:c.164+1dup
ENST00000649850.2:c.164+1dup
ENST00000685018.2:c.164+1dup
ENST00000687278.2:c.164+1dup
ENST00000693465.2:n.249+1dup
ENST00000699585.1:c.164+1dup
ENST00000699596.1:c.164+1dup
ENST00000699597.1:c.164+1dup
ENST00000699598.1:c.164+1dup
ENST00000699599.1:c.164+1dup
ENST00000699600.1:c.164+1dup
ENST00000699601.1:c.164+1dup
ENST00000699602.1:c.164+1dup
ENST00000699604.1:c.164+1dup
ENST00000699605.1:c.-80+1dup
ENST00000446805.2:c.-80+1dup
ENST00000693465.1:n.234+1dup
ENST00000003084.11:c.164+1dup
ENST00000647639.1:n.248+1dup
ENST00000647978.1:c.164+1dup
ENST00000648260.1:c.164+1dup
ENST00000649406.1:c.164+1dup
ENST00000649781.1:c.164+1dup
ENST00000649850.1:n.247+1dup
ENST00000673785.1:c.-80+1dup
ENST00000003084.10:c.164+1dup
ENST00000426809.5:c.164+1dup
ENST00000446805.1:c.-80+1dup
NM_000492.3:c.164+1dup , LRG_663t1:c.164+1dup
XM_011515751.1:c.254+1dup
XM_011515752.1:c.254+1dup
XM_011515753.1:c.-80+1dup
XM_011515754.1:c.-154+1dup
NM_000492.4:c.164+1dup