Canonical Allele Identifier: CA368992574

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117251831T>G (hg19) ; chr7:g.117611777T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117611777T>G , CM000669.2:g.117611777T>G	GRCh38
NC_000007.13:g.117251831T>G , CM000669.1:g.117251831T>G	GRCh37
NC_000007.12:g.117039067T>G	NCBI36
NG_016465.4:g.150994T>G , LRG_663:g.150994T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3336T>G	ENSP00000497673.2:p.Ile1112Met
ENST00000647978.2:c.*3050T>G	ENSP00000497658.1:n.*3050T>G
ENST00000649781.2:c.3153T>G	ENSP00000497203.1:p.Ile1051Met
ENST00000685018.2:c.3336T>G	ENSP00000510194.2:p.Ile1112Met
ENST00000687278.2:c.3336T>G	ENSP00000509593.2:p.Ile1112Met
ENST00000699585.1:c.3336T>G	ENSP00000514456.1:p.Ile1112Met
ENST00000699598.1:c.3336T>G	ENSP00000514467.1:p.Ile1112Met
ENST00000699599.1:c.3336T>G	ENSP00000514468.1:p.Ile1112Met
ENST00000699600.1:c.3336T>G	ENSP00000514469.1:p.Ile1112Met
ENST00000699601.1:c.*1636T>G	ENSP00000514470.1:n.*1636T>G
ENST00000699602.1:c.3336T>G	ENSP00000514471.1:p.Ile1112Met
ENST00000699604.1:c.*3160T>G	ENSP00000514472.1:n.*3160T>G
ENST00000699605.1:c.2910T>G	ENSP00000514473.1:p.Ile970Met
ENST00000685018.1:c.84T>G	ENSP00000510194.1:p.Ile28Met
ENST00000687278.1:c.927T>G	ENSP00000509593.1:p.Ile309Met
ENST00000003084.11:c.3336T>G MANE Select	ENSP00000003084.6:p.Ile1112Met
ENST00000647720.1:c.986T>G
ENST00000648260.1:c.2118T>G	ENSP00000497957.1:p.Ile706Met
ENST00000649406.1:c.3153T>G	ENSP00000497965.1:p.Ile1051Met
ENST00000649781.1:c.3153T>G	ENSP00000497203.1:p.Ile1051Met
ENST00000003084.10:c.3336T>G	ENSP00000003084.6:p.Ile1112Met
ENST00000426809.5:c.3246T>G	ENSP00000389119.1:p.Ile1082Met
ENST00000468795.1:c.161T>G
NM_000492.3:c.3336T>G , LRG_663t1:c.3336T>G	NP_000483.3:p.Ile1112Met
XM_011515751.1:c.3426T>G	XP_011514053.1:p.Ile1142Met
XM_011515752.1:c.3426T>G	XP_011514054.1:p.Ile1142Met
XM_011515753.1:c.3093T>G	XP_011514055.1:p.Ile1031Met
XM_011515754.1:c.3093T>G	XP_011514056.1:p.Ile1031Met
NM_000492.4:c.3336T>G MANE Select	NP_000483.3:p.Ile1112Met