Canonical Allele Identifier: CA368987449

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117243801A>T (hg19) ; chr7:g.117603747A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117603747A>T , CM000669.2:g.117603747A>T	GRCh38
NC_000007.13:g.117243801A>T , CM000669.1:g.117243801A>T	GRCh37
NC_000007.12:g.117031037A>T	NCBI36
NG_016465.4:g.142964A>T , LRG_663:g.142964A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.2873A>T	ENSP00000497673.2:p.Gln958Leu
ENST00000647978.2:c.*2587A>T	ENSP00000497658.1:n.*2587A>T
ENST00000649781.2:c.2690A>T	ENSP00000497203.1:p.Gln897Leu
ENST00000685018.2:c.2873A>T	ENSP00000510194.2:p.Gln958Leu
ENST00000687278.2:c.2873A>T	ENSP00000509593.2:p.Gln958Leu
ENST00000699585.1:c.2873A>T	ENSP00000514456.1:p.Gln958Leu
ENST00000699598.1:c.2873A>T	ENSP00000514467.1:p.Gln958Leu
ENST00000699599.1:c.2873A>T	ENSP00000514468.1:p.Gln958Leu
ENST00000699600.1:c.2873A>T	ENSP00000514469.1:p.Gln958Leu
ENST00000699601.1:c.*1173A>T	ENSP00000514470.1:n.*1173A>T
ENST00000699602.1:c.2873A>T	ENSP00000514471.1:p.Gln958Leu
ENST00000699604.1:c.*2697A>T	ENSP00000514472.1:n.*2697A>T
ENST00000699605.1:c.2447A>T	ENSP00000514473.1:p.Gln816Leu
ENST00000687278.1:c.464A>T	ENSP00000509593.1:p.Gln155Leu
ENST00000003084.11:c.2873A>T MANE Select	ENSP00000003084.6:p.Gln958Leu
ENST00000647720.1:c.523A>T
ENST00000648260.1:c.1655A>T	ENSP00000497957.1:p.Gln552Leu
ENST00000649406.1:c.2690A>T	ENSP00000497965.1:p.Gln897Leu
ENST00000649781.1:c.2690A>T	ENSP00000497203.1:p.Gln897Leu
ENST00000003084.10:c.2873A>T	ENSP00000003084.6:p.Gln958Leu
ENST00000426809.5:c.2783A>T	ENSP00000389119.1:p.Gln928Leu
NM_000492.3:c.2873A>T , LRG_663t1:c.2873A>T	NP_000483.3:p.Gln958Leu
XM_011515751.1:c.2963A>T	XP_011514053.1:p.Gln988Leu
XM_011515752.1:c.2963A>T	XP_011514054.1:p.Gln988Leu
XM_011515753.1:c.2630A>T	XP_011514055.1:p.Gln877Leu
XM_011515754.1:c.2630A>T	XP_011514056.1:p.Gln877Leu
NM_000492.4:c.2873A>T MANE Select	NP_000483.3:p.Gln958Leu