Canonical Allele Identifier: CA368990381

Gene: CFTR

Linked Data

• MyVariant Identifiers: chr7:g.117250595C>A (hg19) ; chr7:g.117610541C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117610541C>A , CM000669.2:g.117610541C>A	GRCh38
NC_000007.13:g.117250595C>A , CM000669.1:g.117250595C>A	GRCh37
NC_000007.12:g.117037831C>A	NCBI36
NG_016465.4:g.149758C>A , LRG_663:g.149758C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647720.2:c.3011C>A	ENSP00000497673.2:p.Ala1004Asp
ENST00000647978.2:c.*2725C>A	ENSP00000497658.1:n.*2725C>A
ENST00000649781.2:c.2828C>A	ENSP00000497203.1:p.Ala943Asp
ENST00000685018.2:c.3011C>A	ENSP00000510194.2:p.Ala1004Asp
ENST00000687278.2:c.3011C>A	ENSP00000509593.2:p.Ala1004Asp
ENST00000699585.1:c.3011C>A	ENSP00000514456.1:p.Ala1004Asp
ENST00000699598.1:c.3011C>A	ENSP00000514467.1:p.Ala1004Asp
ENST00000699599.1:c.3011C>A	ENSP00000514468.1:p.Ala1004Asp
ENST00000699600.1:c.3011C>A	ENSP00000514469.1:p.Ala1004Asp
ENST00000699601.1:c.*1311C>A	ENSP00000514470.1:n.*1311C>A
ENST00000699602.1:c.3011C>A	ENSP00000514471.1:p.Ala1004Asp
ENST00000699604.1:c.*2835C>A	ENSP00000514472.1:n.*2835C>A
ENST00000699605.1:c.2585C>A	ENSP00000514473.1:p.Ala862Asp
ENST00000687278.1:c.602C>A	ENSP00000509593.1:p.Ala201Asp
ENST00000003084.11:c.3011C>A MANE Select	ENSP00000003084.6:p.Ala1004Asp
ENST00000647720.1:c.661C>A
ENST00000648260.1:c.1793C>A	ENSP00000497957.1:p.Ala598Asp
ENST00000649406.1:c.2828C>A	ENSP00000497965.1:p.Ala943Asp
ENST00000649781.1:c.2828C>A	ENSP00000497203.1:p.Ala943Asp
ENST00000003084.10:c.3011C>A	ENSP00000003084.6:p.Ala1004Asp
ENST00000426809.5:c.2921C>A	ENSP00000389119.1:p.Ala974Asp
NM_000492.3:c.3011C>A , LRG_663t1:c.3011C>A	NP_000483.3:p.Ala1004Asp
XM_011515751.1:c.3101C>A	XP_011514053.1:p.Ala1034Asp
XM_011515752.1:c.3101C>A	XP_011514054.1:p.Ala1034Asp
XM_011515753.1:c.2768C>A	XP_011514055.1:p.Ala923Asp
XM_011515754.1:c.2768C>A	XP_011514056.1:p.Ala923Asp
NM_000492.4:c.3011C>A MANE Select	NP_000483.3:p.Ala1004Asp