Canonical Allele Identifier: CA368983825

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117234997A>G (hg19) ; chr7:g.117594943A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117594943A>G , CM000669.2:g.117594943A>G	GRCh38
NC_000007.13:g.117234997A>G , CM000669.1:g.117234997A>G	GRCh37
NC_000007.12:g.117022233A>G	NCBI36
NG_016465.4:g.134160A>G , LRG_663:g.134160A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.2504A>G	ENSP00000497673.2:p.Asp835Gly
ENST00000647978.2:c.*2218A>G	ENSP00000497658.1:n.*2218A>G
ENST00000649781.2:c.2321A>G	ENSP00000497203.1:p.Asp774Gly
ENST00000685018.2:c.2504A>G	ENSP00000510194.2:p.Asp835Gly
ENST00000687278.2:c.2504A>G	ENSP00000509593.2:p.Asp835Gly
ENST00000699585.1:c.2504A>G	ENSP00000514456.1:p.Asp835Gly
ENST00000699598.1:c.2504A>G	ENSP00000514467.1:p.Asp835Gly
ENST00000699599.1:c.2504A>G	ENSP00000514468.1:p.Asp835Gly
ENST00000699600.1:c.2504A>G	ENSP00000514469.1:p.Asp835Gly
ENST00000699601.1:c.*804A>G	ENSP00000514470.1:n.*804A>G
ENST00000699602.1:c.2504A>G	ENSP00000514471.1:p.Asp835Gly
ENST00000699604.1:c.*2328A>G	ENSP00000514472.1:n.*2328A>G
ENST00000699605.1:c.2078A>G	ENSP00000514473.1:p.Asp693Gly
ENST00000687278.1:c.95A>G	ENSP00000509593.1:p.Asp32Gly
ENST00000003084.11:c.2504A>G MANE Select	ENSP00000003084.6:p.Asp835Gly
ENST00000647720.1:c.154A>G
ENST00000647978.1:c.*2218A>G	ENSP00000497658.1:n.*2218A>G
ENST00000648260.1:c.1402-7883A>G	ENSP00000497957.1:n.1402-7883A>G
ENST00000649406.1:c.2321A>G	ENSP00000497965.1:p.Asp774Gly
ENST00000649781.1:c.2321A>G	ENSP00000497203.1:p.Asp774Gly
ENST00000003084.10:c.2504A>G	ENSP00000003084.6:p.Asp835Gly
ENST00000426809.5:c.2414A>G	ENSP00000389119.1:p.Asp805Gly
NM_000492.3:c.2504A>G , LRG_663t1:c.2504A>G	NP_000483.3:p.Asp835Gly
XM_011515751.1:c.2594A>G	XP_011514053.1:p.Asp865Gly
XM_011515752.1:c.2594A>G	XP_011514054.1:p.Asp865Gly
XM_011515753.1:c.2261A>G	XP_011514055.1:p.Asp754Gly
XM_011515754.1:c.2261A>G	XP_011514056.1:p.Asp754Gly
NM_000492.4:c.2504A>G MANE Select	NP_000483.3:p.Asp835Gly