Canonical Allele Identifier: CA457230174

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117254698G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117614644G>C , CM000669.2:g.117614644G>C	GRCh38
NC_000007.13:g.117254698G>C , CM000669.1:g.117254698G>C	GRCh37
NC_000007.12:g.117041934G>C	NCBI36
NG_016465.4:g.153861G>C , LRG_663:g.153861G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3399G>C	ENSP00000497673.2:p.Leu1133=
ENST00000647978.2:c.*3113G>C	ENSP00000497658.1:n.*3113G>C
ENST00000649781.2:c.3216G>C	ENSP00000497203.1:p.Leu1072=
ENST00000685018.2:c.3399G>C	ENSP00000510194.2:p.Leu1133=
ENST00000687278.2:c.3399G>C	ENSP00000509593.2:p.Leu1133=
ENST00000699585.1:c.3399G>C	ENSP00000514456.1:p.Leu1133=
ENST00000699598.1:c.3399G>C	ENSP00000514467.1:p.Leu1133=
ENST00000699599.1:c.3399G>C	ENSP00000514468.1:p.Leu1133=
ENST00000699600.1:c.3399G>C	ENSP00000514469.1:p.Leu1133=
ENST00000699601.1:c.*1774G>C	ENSP00000514470.1:n.*1774G>C
ENST00000699602.1:c.3393G>C	ENSP00000514471.1:p.Leu1131=
ENST00000699604.1:c.*3223G>C	ENSP00000514472.1:n.*3223G>C
ENST00000699605.1:c.2973G>C	ENSP00000514473.1:p.Leu991=
ENST00000685018.1:c.147G>C	ENSP00000510194.1:p.Leu49=
ENST00000687278.1:c.990G>C	ENSP00000509593.1:p.Leu330=
ENST00000003084.11:c.3399G>C MANE Select	ENSP00000003084.6:p.Leu1133=
ENST00000647720.1:c.1049G>C
ENST00000648260.1:c.2181G>C	ENSP00000497957.1:p.Leu727=
ENST00000649406.1:c.3216G>C	ENSP00000497965.1:p.Leu1072=
ENST00000649781.1:c.3216G>C	ENSP00000497203.1:p.Leu1072=
ENST00000003084.10:c.3399G>C	ENSP00000003084.6:p.Leu1133=
ENST00000426809.5:c.3309G>C	ENSP00000389119.1:p.Leu1103=
ENST00000468795.1:c.224G>C
NM_000492.3:c.3399G>C , LRG_663t1:c.3399G>C	NP_000483.3:p.Leu1133=
XM_011515751.1:c.3489G>C	XP_011514053.1:p.Leu1163=
XM_011515752.1:c.3489G>C	XP_011514054.1:p.Leu1163=
XM_011515753.1:c.3156G>C	XP_011514055.1:p.Leu1052=
XM_011515754.1:c.3156G>C	XP_011514056.1:p.Leu1052=
NM_000492.4:c.3399G>C MANE Select	NP_000483.3:p.Leu1133=