Canonical Allele Identifier: CA457227386

Gene: CFTR

Linked Data

• ClinVar Variation Id: 2453647
• ClinVar RCV Id: RCV003187782
• gnomAD v4: 7-117504289-G-A
• MyVariant Identifiers: chr7:g.117144343G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117504289G>A , CM000669.2:g.117504289G>A	GRCh38
NC_000007.13:g.117144343G>A , CM000669.1:g.117144343G>A	GRCh37
NC_000007.12:g.116931579G>A	NCBI36
NG_016465.4:g.43506G>A , LRG_663:g.43506G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.90G>A	ENSP00000497673.2:p.Gln30=
ENST00000647978.2:c.90G>A	ENSP00000497658.1:p.Gln30=
ENST00000649781.2:c.90G>A	ENSP00000497203.1:p.Gln30=
ENST00000649850.2:c.90G>A	ENSP00000514457.1:p.Gln30=
ENST00000685018.2:c.90G>A	ENSP00000510194.2:p.Gln30=
ENST00000687278.2:c.90G>A	ENSP00000509593.2:p.Gln30=
ENST00000693465.2:n.175G>A
ENST00000699585.1:c.90G>A	ENSP00000514456.1:p.Gln30=
ENST00000699596.1:c.90G>A	ENSP00000514465.1:p.Gln30=
ENST00000699597.1:c.90G>A	ENSP00000514466.1:p.Gln30=
ENST00000699598.1:c.90G>A	ENSP00000514467.1:p.Gln30=
ENST00000699599.1:c.90G>A	ENSP00000514468.1:p.Gln30=
ENST00000699600.1:c.90G>A	ENSP00000514469.1:p.Gln30=
ENST00000699601.1:c.90G>A	ENSP00000514470.1:p.Gln30=
ENST00000699602.1:c.90G>A	ENSP00000514471.1:p.Gln30=
ENST00000699604.1:c.90G>A	ENSP00000514472.1:p.Gln30=
ENST00000699605.1:c.-154G>A	ENSP00000514473.1:n.-154G>A
ENST00000446805.2:c.-154G>A	ENSP00000417012.1:n.-154G>A
ENST00000693465.1:n.160G>A
ENST00000003084.11:c.90G>A MANE Select	ENSP00000003084.6:p.Gln30=
ENST00000647639.1:n.174G>A
ENST00000647978.1:c.90G>A	ENSP00000497658.1:p.Gln30=
ENST00000648260.1:c.90G>A	ENSP00000497957.1:p.Gln30=
ENST00000649406.1:c.90G>A	ENSP00000497965.1:p.Gln30=
ENST00000649781.1:c.90G>A	ENSP00000497203.1:p.Gln30=
ENST00000649850.1:n.173G>A
ENST00000673785.1:c.-154G>A	ENSP00000501235.1:n.-154G>A
ENST00000003084.10:c.90G>A	ENSP00000003084.6:p.Gln30=
ENST00000426809.5:c.90G>A	ENSP00000389119.1:p.Gln30=
ENST00000446805.1:c.-154G>A	ENSP00000417012.1:n.-154G>A
ENST00000546407.1:n.203G>A
NM_000492.3:c.90G>A , LRG_663t1:c.90G>A	NP_000483.3:p.Gln30=
XM_011515751.1:c.180G>A	XP_011514053.1:p.Gln60=
XM_011515752.1:c.180G>A	XP_011514054.1:p.Gln60=
XM_011515753.1:c.-154G>A	XP_011514055.1:n.-154G>A
XM_011515754.1:c.-228G>A	XP_011514056.1:n.-228G>A
NM_000492.4:c.90G>A MANE Select	NP_000483.3:p.Gln30=