Canonical Allele Identifier: CA368996356

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117267656G>T (hg19) ; chr7:g.117627602G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117627602G>T , CM000669.2:g.117627602G>T	GRCh38
NC_000007.13:g.117267656G>T , CM000669.1:g.117267656G>T	GRCh37
NC_000007.12:g.117054892G>T	NCBI36
NG_016465.4:g.166819G>T , LRG_663:g.166819G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3517+32G>T	ENSP00000497673.2:n.3517+32G>T
ENST00000647978.2:c.*3263G>T	ENSP00000497658.1:n.*3263G>T
ENST00000649781.2:c.3366G>T	ENSP00000497203.1:p.Lys1122Asn
ENST00000685018.2:c.3549G>T	ENSP00000510194.2:p.Lys1183Asn
ENST00000687278.2:c.*202G>T	ENSP00000509593.2:n.*202G>T
ENST00000699585.1:c.3517+32G>T	ENSP00000514456.1:n.3517+32G>T
ENST00000699598.1:c.3549G>T	ENSP00000514467.1:p.Lys1183Asn
ENST00000699599.1:c.3549G>T	ENSP00000514468.1:p.Lys1183Asn
ENST00000699600.1:c.*210G>T	ENSP00000514469.1:n.*210G>T
ENST00000699601.1:c.*1924G>T	ENSP00000514470.1:n.*1924G>T
ENST00000699602.1:c.3543G>T	ENSP00000514471.1:p.Lys1181Asn
ENST00000699604.1:c.*3373G>T	ENSP00000514472.1:n.*3373G>T
ENST00000699605.1:c.3123G>T	ENSP00000514473.1:p.Lys1041Asn
ENST00000685018.1:c.297G>T	ENSP00000510194.1:p.Lys99Asn
ENST00000687278.1:c.1336G>T	ENSP00000509593.1:n.1336G>T
ENST00000689011.1:c.131G>T
ENST00000003084.11:c.3549G>T MANE Select	ENSP00000003084.6:p.Lys1183Asn
ENST00000647720.1:c.1167+32G>T
ENST00000648260.1:c.2331G>T	ENSP00000497957.1:p.Lys777Asn
ENST00000649406.1:c.3366G>T	ENSP00000497965.1:p.Lys1122Asn
ENST00000649781.1:c.3366G>T	ENSP00000497203.1:p.Lys1122Asn
ENST00000003084.10:c.3549G>T	ENSP00000003084.6:p.Lys1183Asn
ENST00000426809.5:c.3459G>T	ENSP00000389119.1:p.Lys1153Asn
ENST00000468795.1:c.374G>T
NM_000492.3:c.3549G>T , LRG_663t1:c.3549G>T	NP_000483.3:p.Lys1183Asn
XM_011515751.1:c.3639G>T	XP_011514053.1:p.Lys1213Asn
XM_011515752.1:c.3639G>T	XP_011514054.1:p.Lys1213Asn
XM_011515753.1:c.3306G>T	XP_011514055.1:p.Lys1102Asn
XM_011515754.1:c.3306G>T	XP_011514056.1:p.Lys1102Asn
NM_000492.4:c.3549G>T MANE Select	NP_000483.3:p.Lys1183Asn