Canonical Allele Identifier: CA368992089

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117251703C>G (hg19) ; chr7:g.117611649C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611649C>G , CM000669.2:g.117611649C>G	GRCh38
NC_000007.13:g.117251703C>G , CM000669.1:g.117251703C>G	GRCh37
NC_000007.12:g.117038939C>G	NCBI36
NG_016465.4:g.150866C>G , LRG_663:g.150866C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3208C>G	ENSP00000497673.2:p.Arg1070Gly
ENST00000647978.2:c.*2922C>G	ENSP00000497658.1:n.*2922C>G
ENST00000649781.2:c.3025C>G	ENSP00000497203.1:p.Arg1009Gly
ENST00000685018.2:c.3208C>G	ENSP00000510194.2:p.Arg1070Gly
ENST00000687278.2:c.3208C>G	ENSP00000509593.2:p.Arg1070Gly
ENST00000699585.1:c.3208C>G	ENSP00000514456.1:p.Arg1070Gly
ENST00000699598.1:c.3208C>G	ENSP00000514467.1:p.Arg1070Gly
ENST00000699599.1:c.3208C>G	ENSP00000514468.1:p.Arg1070Gly
ENST00000699600.1:c.3208C>G	ENSP00000514469.1:p.Arg1070Gly
ENST00000699601.1:c.*1508C>G	ENSP00000514470.1:n.*1508C>G
ENST00000699602.1:c.3208C>G	ENSP00000514471.1:p.Arg1070Gly
ENST00000699604.1:c.*3032C>G	ENSP00000514472.1:n.*3032C>G
ENST00000699605.1:c.2782C>G	ENSP00000514473.1:p.Arg928Gly
ENST00000687278.1:c.799C>G	ENSP00000509593.1:p.Arg267Gly
ENST00000003084.11:c.3208C>G MANE Select	ENSP00000003084.6:p.Arg1070Gly
ENST00000647720.1:c.858C>G
ENST00000648260.1:c.1990C>G	ENSP00000497957.1:p.Arg664Gly
ENST00000649406.1:c.3025C>G	ENSP00000497965.1:p.Arg1009Gly
ENST00000649781.1:c.3025C>G	ENSP00000497203.1:p.Arg1009Gly
ENST00000003084.10:c.3208C>G	ENSP00000003084.6:p.Arg1070Gly
ENST00000426809.5:c.3118C>G	ENSP00000389119.1:p.Arg1040Gly
ENST00000468795.1:c.33C>G
NM_000492.3:c.3208C>G , LRG_663t1:c.3208C>G	NP_000483.3:p.Arg1070Gly
XM_011515751.1:c.3298C>G	XP_011514053.1:p.Arg1100Gly
XM_011515752.1:c.3298C>G	XP_011514054.1:p.Arg1100Gly
XM_011515753.1:c.2965C>G	XP_011514055.1:p.Arg989Gly
XM_011515754.1:c.2965C>G	XP_011514056.1:p.Arg989Gly
NM_000492.4:c.3208C>G MANE Select	NP_000483.3:p.Arg1070Gly