Canonical Allele Identifier: CA368981851

Gene: CFTR CFTR-AS1

Linked Data

• dbSNP Id: rs2115903382
• MyVariant Identifiers: chr7:g.117188791C>G (hg19) ; chr7:g.117548737C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117548737C>G , CM000669.2:g.117548737C>G	GRCh38
NC_000007.13:g.117188791C>G , CM000669.1:g.117188791C>G	GRCh37
NC_000007.12:g.116976027C>G	NCBI36
NG_016465.4:g.87954C>G , LRG_663:g.87954C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.1306C>G (CFTR)	ENSP00000497673.2:p.Leu436Val
ENST00000647978.2:c.*1106+6629C>G (CFTR)	ENSP00000497658.1:n.*1106+6629C>G
ENST00000649781.2:c.1209+6629C>G (CFTR)	ENSP00000497203.1:n.1209+6629C>G
ENST00000685018.2:c.1306C>G (CFTR)	ENSP00000510194.2:p.Leu436Val
ENST00000687278.2:c.1306C>G (CFTR)	ENSP00000509593.2:p.Leu436Val
ENST00000699585.1:c.1306C>G (CFTR)	ENSP00000514456.1:p.Leu436Val
ENST00000699596.1:c.1306C>G (CFTR)	ENSP00000514465.1:p.Leu436Val
ENST00000699597.1:c.1306C>G (CFTR)	ENSP00000514466.1:p.Leu436Val
ENST00000699598.1:c.1306C>G (CFTR)	ENSP00000514467.1:p.Leu436Val
ENST00000699599.1:c.1306C>G (CFTR)	ENSP00000514468.1:p.Leu436Val
ENST00000699600.1:c.1306C>G (CFTR)	ENSP00000514469.1:p.Leu436Val
ENST00000699601.1:c.1306C>G (CFTR)	ENSP00000514470.1:p.Leu436Val
ENST00000699602.1:c.1306C>G (CFTR)	ENSP00000514471.1:p.Leu436Val
ENST00000699604.1:c.*1130C>G (CFTR)	ENSP00000514472.1:n.*1130C>G
ENST00000699605.1:c.966+6629C>G (CFTR)	ENSP00000514473.1:n.966+6629C>G
ENST00000003084.11:c.1306C>G (CFTR) MANE Select	ENSP00000003084.6:p.Leu436Val
ENST00000647978.1:c.*1106+6629C>G (CFTR)	ENSP00000497658.1:n.*1106+6629C>G
ENST00000648260.1:c.1209+6629C>G (CFTR)	ENSP00000497957.1:n.1209+6629C>G
ENST00000649406.1:c.1209+6629C>G (CFTR)	ENSP00000497965.1:n.1209+6629C>G
ENST00000649781.1:c.1209+6629C>G (CFTR)	ENSP00000497203.1:n.1209+6629C>G
ENST00000003084.10:c.1306C>G (CFTR)	ENSP00000003084.6:p.Leu436Val
ENST00000426809.5:c.1216C>G (CFTR)	ENSP00000389119.1:p.Leu406Val
NM_000492.3:c.1306C>G , LRG_663t1:c.1306C>G (CFTR)	NP_000483.3:p.Leu436Val
XM_011515751.1:c.1396C>G (CFTR)	XP_011514053.1:p.Leu466Val
XM_011515752.1:c.1396C>G (CFTR)	XP_011514054.1:p.Leu466Val
XM_011515753.1:c.1063C>G (CFTR)	XP_011514055.1:p.Leu355Val
XM_011515754.1:c.1063C>G (CFTR)	XP_011514056.1:p.Leu355Val
NR_149084.1:n.222-6198G>C (CFTR-AS1)
NM_000492.4:c.1306C>G (CFTR) MANE Select	NP_000483.3:p.Leu436Val