Canonical Allele Identifier: CA368974818

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117282555C>A (hg19) ; chr7:g.117642501C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117642501C>A , CM000669.2:g.117642501C>A	GRCh38
NC_000007.13:g.117282555C>A , CM000669.1:g.117282555C>A	GRCh37
NC_000007.12:g.117069791C>A	NCBI36
NG_016465.4:g.181718C>A , LRG_663:g.181718C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3581C>A	ENSP00000497673.2:p.Thr1194Asn
ENST00000647978.2:c.*3495C>A	ENSP00000497658.1:n.*3495C>A
ENST00000649781.2:c.3598C>A	ENSP00000497203.1:p.Leu1200Met
ENST00000685018.2:c.3781C>A	ENSP00000510194.2:p.Leu1261Met
ENST00000687278.2:c.*434C>A	ENSP00000509593.2:n.*434C>A
ENST00000699585.1:c.3581C>A	ENSP00000514456.1:p.Thr1194Asn
ENST00000699598.1:c.3781C>A	ENSP00000514467.1:p.Leu1261Met
ENST00000699599.1:c.3781C>A	ENSP00000514468.1:p.Leu1261Met
ENST00000699600.1:c.*442C>A	ENSP00000514469.1:n.*442C>A
ENST00000699601.1:c.*2156C>A	ENSP00000514470.1:n.*2156C>A
ENST00000699602.1:c.3775C>A	ENSP00000514471.1:p.Leu1259Met
ENST00000699604.1:c.*3605C>A	ENSP00000514472.1:n.*3605C>A
ENST00000699605.1:c.3355C>A	ENSP00000514473.1:p.Leu1119Met
ENST00000685018.1:c.529C>A	ENSP00000510194.1:p.Leu177Met
ENST00000687278.1:c.1568C>A	ENSP00000509593.1:n.1568C>A
ENST00000689011.1:c.363C>A
ENST00000003084.11:c.3781C>A MANE Select	ENSP00000003084.6:p.Leu1261Met
ENST00000647720.1:c.1231C>A
ENST00000649781.1:c.3598C>A	ENSP00000497203.1:p.Leu1200Met
ENST00000003084.10:c.3781C>A	ENSP00000003084.6:p.Leu1261Met
ENST00000426809.5:c.3691C>A	ENSP00000389119.1:p.Leu1231Met
NM_000492.3:c.3781C>A , LRG_663t1:c.3781C>A	NP_000483.3:p.Leu1261Met
XM_011515751.1:c.3871C>A	XP_011514053.1:p.Leu1291Met
XM_011515752.1:c.3871C>A	XP_011514054.1:p.Leu1291Met
XM_011515753.1:c.3538C>A	XP_011514055.1:p.Leu1180Met
XM_011515754.1:c.3538C>A	XP_011514056.1:p.Leu1180Met
NM_000492.4:c.3781C>A MANE Select	NP_000483.3:p.Leu1261Met