Canonical Allele Identifier: CA368996373

Gene: CFTR

Linked Data

• gnomAD v4: 7-117627606-G-A
• MyVariant Identifiers: chr7:g.117267660G>A (hg19) ; chr7:g.117627606G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117627606G>A , CM000669.2:g.117627606G>A	GRCh38
NC_000007.13:g.117267660G>A , CM000669.1:g.117267660G>A	GRCh37
NC_000007.12:g.117054896G>A	NCBI36
NG_016465.4:g.166823G>A , LRG_663:g.166823G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3517+36G>A	ENSP00000497673.2:n.3517+36G>A
ENST00000647978.2:c.*3267G>A	ENSP00000497658.1:n.*3267G>A
ENST00000649781.2:c.3370G>A	ENSP00000497203.1:p.Gly1124Ser
ENST00000685018.2:c.3553G>A	ENSP00000510194.2:p.Gly1185Ser
ENST00000687278.2:c.*206G>A	ENSP00000509593.2:n.*206G>A
ENST00000699585.1:c.3517+36G>A	ENSP00000514456.1:n.3517+36G>A
ENST00000699598.1:c.3553G>A	ENSP00000514467.1:p.Gly1185Ser
ENST00000699599.1:c.3553G>A	ENSP00000514468.1:p.Gly1185Ser
ENST00000699600.1:c.*214G>A	ENSP00000514469.1:n.*214G>A
ENST00000699601.1:c.*1928G>A	ENSP00000514470.1:n.*1928G>A
ENST00000699602.1:c.3547G>A	ENSP00000514471.1:p.Gly1183Ser
ENST00000699604.1:c.*3377G>A	ENSP00000514472.1:n.*3377G>A
ENST00000699605.1:c.3127G>A	ENSP00000514473.1:p.Gly1043Ser
ENST00000685018.1:c.301G>A	ENSP00000510194.1:p.Gly101Ser
ENST00000687278.1:c.1340G>A	ENSP00000509593.1:n.1340G>A
ENST00000689011.1:c.135G>A
ENST00000003084.11:c.3553G>A MANE Select	ENSP00000003084.6:p.Gly1185Ser
ENST00000647720.1:c.1167+36G>A
ENST00000648260.1:c.2335G>A	ENSP00000497957.1:p.Gly779Ser
ENST00000649406.1:c.3370G>A	ENSP00000497965.1:p.Gly1124Ser
ENST00000649781.1:c.3370G>A	ENSP00000497203.1:p.Gly1124Ser
ENST00000003084.10:c.3553G>A	ENSP00000003084.6:p.Gly1185Ser
ENST00000426809.5:c.3463G>A	ENSP00000389119.1:p.Gly1155Ser
ENST00000468795.1:c.378G>A
NM_000492.3:c.3553G>A , LRG_663t1:c.3553G>A	NP_000483.3:p.Gly1185Ser
XM_011515751.1:c.3643G>A	XP_011514053.1:p.Gly1215Ser
XM_011515752.1:c.3643G>A	XP_011514054.1:p.Gly1215Ser
XM_011515753.1:c.3310G>A	XP_011514055.1:p.Gly1104Ser
XM_011515754.1:c.3310G>A	XP_011514056.1:p.Gly1104Ser
NM_000492.4:c.3553G>A MANE Select	NP_000483.3:p.Gly1185Ser