Canonical Allele Identifier: CA368997298

Gene: CFTR

Linked Data

• dbSNP Id: rs1221344688
• MyVariant Identifiers: chr7:g.117267747G>A (hg19) ; chr7:g.117627693G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117627693G>A , CM000669.2:g.117627693G>A	GRCh38
NC_000007.13:g.117267747G>A , CM000669.1:g.117267747G>A	GRCh37
NC_000007.12:g.117054983G>A	NCBI36
NG_016465.4:g.166910G>A , LRG_663:g.166910G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3517+123G>A	ENSP00000497673.2:n.3517+123G>A
ENST00000647978.2:c.*3354G>A	ENSP00000497658.1:n.*3354G>A
ENST00000649781.2:c.3457G>A	ENSP00000497203.1:p.Asp1153Asn
ENST00000685018.2:c.3640G>A	ENSP00000510194.2:p.Asp1214Asn
ENST00000687278.2:c.*293G>A	ENSP00000509593.2:n.*293G>A
ENST00000699585.1:c.3517+123G>A	ENSP00000514456.1:n.3517+123G>A
ENST00000699598.1:c.3640G>A	ENSP00000514467.1:p.Asp1214Asn
ENST00000699599.1:c.3640G>A	ENSP00000514468.1:p.Asp1214Asn
ENST00000699600.1:c.*301G>A	ENSP00000514469.1:n.*301G>A
ENST00000699601.1:c.*2015G>A	ENSP00000514470.1:n.*2015G>A
ENST00000699602.1:c.3634G>A	ENSP00000514471.1:p.Asp1212Asn
ENST00000699604.1:c.*3464G>A	ENSP00000514472.1:n.*3464G>A
ENST00000699605.1:c.3214G>A	ENSP00000514473.1:p.Asp1072Asn
ENST00000685018.1:c.388G>A	ENSP00000510194.1:p.Asp130Asn
ENST00000687278.1:c.1427G>A	ENSP00000509593.1:n.1427G>A
ENST00000689011.1:c.222G>A
ENST00000003084.11:c.3640G>A MANE Select	ENSP00000003084.6:p.Asp1214Asn
ENST00000647720.1:c.1167+123G>A
ENST00000648260.1:c.2422G>A	ENSP00000497957.1:p.Asp808Asn
ENST00000649406.1:c.3457G>A	ENSP00000497965.1:p.Asp1153Asn
ENST00000649781.1:c.3457G>A	ENSP00000497203.1:p.Asp1153Asn
ENST00000003084.10:c.3640G>A	ENSP00000003084.6:p.Asp1214Asn
ENST00000426809.5:c.3550G>A	ENSP00000389119.1:p.Asp1184Asn
ENST00000468795.1:c.465G>A
NM_000492.3:c.3640G>A , LRG_663t1:c.3640G>A	NP_000483.3:p.Asp1214Asn
XM_011515751.1:c.3730G>A	XP_011514053.1:p.Asp1244Asn
XM_011515752.1:c.3730G>A	XP_011514054.1:p.Asp1244Asn
XM_011515753.1:c.3397G>A	XP_011514055.1:p.Asp1133Asn
XM_011515754.1:c.3397G>A	XP_011514056.1:p.Asp1133Asn
NM_000492.4:c.3640G>A MANE Select	NP_000483.3:p.Asp1214Asn