Canonical Allele Identifier: CA368974469

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117282508G>T (hg19) ; chr7:g.117642454G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117642454G>T , CM000669.2:g.117642454G>T	GRCh38
NC_000007.13:g.117282508G>T , CM000669.1:g.117282508G>T	GRCh37
NC_000007.12:g.117069744G>T	NCBI36
NG_016465.4:g.181671G>T , LRG_663:g.181671G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3534G>T	ENSP00000497673.2:p.Lys1178Asn
ENST00000647978.2:c.*3448G>T	ENSP00000497658.1:n.*3448G>T
ENST00000649781.2:c.3551G>T	ENSP00000497203.1:p.Arg1184Ile
ENST00000685018.2:c.3734G>T	ENSP00000510194.2:p.Arg1245Ile
ENST00000687278.2:c.*387G>T	ENSP00000509593.2:n.*387G>T
ENST00000699585.1:c.3534G>T	ENSP00000514456.1:p.Lys1178Asn
ENST00000699598.1:c.3734G>T	ENSP00000514467.1:p.Arg1245Ile
ENST00000699599.1:c.3734G>T	ENSP00000514468.1:p.Arg1245Ile
ENST00000699600.1:c.*395G>T	ENSP00000514469.1:n.*395G>T
ENST00000699601.1:c.*2109G>T	ENSP00000514470.1:n.*2109G>T
ENST00000699602.1:c.3728G>T	ENSP00000514471.1:p.Arg1243Ile
ENST00000699604.1:c.*3558G>T	ENSP00000514472.1:n.*3558G>T
ENST00000699605.1:c.3308G>T	ENSP00000514473.1:p.Arg1103Ile
ENST00000685018.1:c.482G>T	ENSP00000510194.1:p.Arg161Ile
ENST00000687278.1:c.1521G>T	ENSP00000509593.1:n.1521G>T
ENST00000689011.1:c.316G>T
ENST00000003084.11:c.3734G>T MANE Select	ENSP00000003084.6:p.Arg1245Ile
ENST00000647720.1:c.1184G>T
ENST00000649781.1:c.3551G>T	ENSP00000497203.1:p.Arg1184Ile
ENST00000003084.10:c.3734G>T	ENSP00000003084.6:p.Arg1245Ile
ENST00000426809.5:c.3644G>T	ENSP00000389119.1:p.Arg1215Ile
NM_000492.3:c.3734G>T , LRG_663t1:c.3734G>T	NP_000483.3:p.Arg1245Ile
XM_011515751.1:c.3824G>T	XP_011514053.1:p.Arg1275Ile
XM_011515752.1:c.3824G>T	XP_011514054.1:p.Arg1275Ile
XM_011515753.1:c.3491G>T	XP_011514055.1:p.Arg1164Ile
XM_011515754.1:c.3491G>T	XP_011514056.1:p.Arg1164Ile
NM_000492.4:c.3734G>T MANE Select	NP_000483.3:p.Arg1245Ile