Canonical Allele Identifier: CA368986980

Gene: CFTR

Linked Data

• ClinVar Variation Id: 1796330
• ClinVar RCV Id: RCV002441704
• MyVariant Identifiers: chr7:g.117243738T>C (hg19) ; chr7:g.117603684T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603684T>C , CM000669.2:g.117603684T>C	GRCh38
NC_000007.13:g.117243738T>C , CM000669.1:g.117243738T>C	GRCh37
NC_000007.12:g.117030974T>C	NCBI36
NG_016465.4:g.142901T>C , LRG_663:g.142901T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.2810T>C	ENSP00000497673.2:p.Leu937Pro
ENST00000647978.2:c.*2524T>C	ENSP00000497658.1:n.*2524T>C
ENST00000649781.2:c.2627T>C	ENSP00000497203.1:p.Leu876Pro
ENST00000685018.2:c.2810T>C	ENSP00000510194.2:p.Leu937Pro
ENST00000687278.2:c.2810T>C	ENSP00000509593.2:p.Leu937Pro
ENST00000699585.1:c.2810T>C	ENSP00000514456.1:p.Leu937Pro
ENST00000699598.1:c.2810T>C	ENSP00000514467.1:p.Leu937Pro
ENST00000699599.1:c.2810T>C	ENSP00000514468.1:p.Leu937Pro
ENST00000699600.1:c.2810T>C	ENSP00000514469.1:p.Leu937Pro
ENST00000699601.1:c.*1110T>C	ENSP00000514470.1:n.*1110T>C
ENST00000699602.1:c.2810T>C	ENSP00000514471.1:p.Leu937Pro
ENST00000699604.1:c.*2634T>C	ENSP00000514472.1:n.*2634T>C
ENST00000699605.1:c.2384T>C	ENSP00000514473.1:p.Leu795Pro
ENST00000687278.1:c.401T>C	ENSP00000509593.1:p.Leu134Pro
ENST00000003084.11:c.2810T>C MANE Select	ENSP00000003084.6:p.Leu937Pro
ENST00000647720.1:c.460T>C
ENST00000648260.1:c.1592T>C	ENSP00000497957.1:p.Leu531Pro
ENST00000649406.1:c.2627T>C	ENSP00000497965.1:p.Leu876Pro
ENST00000649781.1:c.2627T>C	ENSP00000497203.1:p.Leu876Pro
ENST00000003084.10:c.2810T>C	ENSP00000003084.6:p.Leu937Pro
ENST00000426809.5:c.2720T>C	ENSP00000389119.1:p.Leu907Pro
NM_000492.3:c.2810T>C , LRG_663t1:c.2810T>C	NP_000483.3:p.Leu937Pro
XM_011515751.1:c.2900T>C	XP_011514053.1:p.Leu967Pro
XM_011515752.1:c.2900T>C	XP_011514054.1:p.Leu967Pro
XM_011515753.1:c.2567T>C	XP_011514055.1:p.Leu856Pro
XM_011515754.1:c.2567T>C	XP_011514056.1:p.Leu856Pro
NM_000492.4:c.2810T>C MANE Select	NP_000483.3:p.Leu937Pro