Canonical Allele Identifier: CA457230212

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117254761T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117614707T>C , CM000669.2:g.117614707T>C	GRCh38
NC_000007.13:g.117254761T>C , CM000669.1:g.117254761T>C	GRCh37
NC_000007.12:g.117041997T>C	NCBI36
NG_016465.4:g.153924T>C , LRG_663:g.153924T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3462T>C	ENSP00000497673.2:p.Asp1154=
ENST00000647978.2:c.*3176T>C	ENSP00000497658.1:n.*3176T>C
ENST00000649781.2:c.3279T>C	ENSP00000497203.1:p.Asp1093=
ENST00000685018.2:c.3462T>C	ENSP00000510194.2:p.Asp1154=
ENST00000687278.2:c.3462T>C	ENSP00000509593.2:p.Asp1154=
ENST00000699585.1:c.3462T>C	ENSP00000514456.1:p.Asp1154=
ENST00000699598.1:c.3462T>C	ENSP00000514467.1:p.Asp1154=
ENST00000699599.1:c.3462T>C	ENSP00000514468.1:p.Asp1154=
ENST00000699600.1:c.3462T>C	ENSP00000514469.1:p.Asp1154=
ENST00000699601.1:c.*1837T>C	ENSP00000514470.1:n.*1837T>C
ENST00000699602.1:c.3456T>C	ENSP00000514471.1:p.Asp1152=
ENST00000699604.1:c.*3286T>C	ENSP00000514472.1:n.*3286T>C
ENST00000699605.1:c.3036T>C	ENSP00000514473.1:p.Asp1012=
ENST00000685018.1:c.210T>C	ENSP00000510194.1:p.Asp70=
ENST00000687278.1:c.1053T>C	ENSP00000509593.1:p.Asp351=
ENST00000689011.1:c.44T>C
ENST00000003084.11:c.3462T>C MANE Select	ENSP00000003084.6:p.Asp1154=
ENST00000647720.1:c.1112T>C
ENST00000648260.1:c.2244T>C	ENSP00000497957.1:p.Asp748=
ENST00000649406.1:c.3279T>C	ENSP00000497965.1:p.Asp1093=
ENST00000649781.1:c.3279T>C	ENSP00000497203.1:p.Asp1093=
ENST00000003084.10:c.3462T>C	ENSP00000003084.6:p.Asp1154=
ENST00000426809.5:c.3372T>C	ENSP00000389119.1:p.Asp1124=
ENST00000468795.1:c.287T>C
NM_000492.3:c.3462T>C , LRG_663t1:c.3462T>C	NP_000483.3:p.Asp1154=
XM_011515751.1:c.3552T>C	XP_011514053.1:p.Asp1184=
XM_011515752.1:c.3552T>C	XP_011514054.1:p.Asp1184=
XM_011515753.1:c.3219T>C	XP_011514055.1:p.Asp1073=
XM_011515754.1:c.3219T>C	XP_011514056.1:p.Asp1073=
NM_000492.4:c.3462T>C MANE Select	NP_000483.3:p.Asp1154=