Canonical Allele Identifier: CA368990510

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117250616T>C (hg19) ; chr7:g.117610562T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117610562T>C , CM000669.2:g.117610562T>C	GRCh38
NC_000007.13:g.117250616T>C , CM000669.1:g.117250616T>C	GRCh37
NC_000007.12:g.117037852T>C	NCBI36
NG_016465.4:g.149779T>C , LRG_663:g.149779T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3032T>C	ENSP00000497673.2:p.Leu1011Ser
ENST00000647978.2:c.*2746T>C	ENSP00000497658.1:n.*2746T>C
ENST00000649781.2:c.2849T>C	ENSP00000497203.1:p.Leu950Ser
ENST00000685018.2:c.3032T>C	ENSP00000510194.2:p.Leu1011Ser
ENST00000687278.2:c.3032T>C	ENSP00000509593.2:p.Leu1011Ser
ENST00000699585.1:c.3032T>C	ENSP00000514456.1:p.Leu1011Ser
ENST00000699598.1:c.3032T>C	ENSP00000514467.1:p.Leu1011Ser
ENST00000699599.1:c.3032T>C	ENSP00000514468.1:p.Leu1011Ser
ENST00000699600.1:c.3032T>C	ENSP00000514469.1:p.Leu1011Ser
ENST00000699601.1:c.*1332T>C	ENSP00000514470.1:n.*1332T>C
ENST00000699602.1:c.3032T>C	ENSP00000514471.1:p.Leu1011Ser
ENST00000699604.1:c.*2856T>C	ENSP00000514472.1:n.*2856T>C
ENST00000699605.1:c.2606T>C	ENSP00000514473.1:p.Leu869Ser
ENST00000687278.1:c.623T>C	ENSP00000509593.1:p.Leu208Ser
ENST00000003084.11:c.3032T>C MANE Select	ENSP00000003084.6:p.Leu1011Ser
ENST00000647720.1:c.682T>C
ENST00000648260.1:c.1814T>C	ENSP00000497957.1:p.Leu605Ser
ENST00000649406.1:c.2849T>C	ENSP00000497965.1:p.Leu950Ser
ENST00000649781.1:c.2849T>C	ENSP00000497203.1:p.Leu950Ser
ENST00000003084.10:c.3032T>C	ENSP00000003084.6:p.Leu1011Ser
ENST00000426809.5:c.2942T>C	ENSP00000389119.1:p.Leu981Ser
NM_000492.3:c.3032T>C , LRG_663t1:c.3032T>C	NP_000483.3:p.Leu1011Ser
XM_011515751.1:c.3122T>C	XP_011514053.1:p.Leu1041Ser
XM_011515752.1:c.3122T>C	XP_011514054.1:p.Leu1041Ser
XM_011515753.1:c.2789T>C	XP_011514055.1:p.Leu930Ser
XM_011515754.1:c.2789T>C	XP_011514056.1:p.Leu930Ser
NM_000492.4:c.3032T>C MANE Select	NP_000483.3:p.Leu1011Ser