Canonical Allele Identifier: CA577223235

Gene: CFTR

Linked Data

• dbSNP Id: rs1379996837
• gnomAD v2: 7-117267407-T-TGGATA
• gnomAD v3: 7-117627353-T-TGGATA
• gnomAD v4: 7-117627353-T-TGGATA
• MyVariant Identifiers: chr7:g.117267407_117267408insGGATA (hg19) ; chr7:g.117627353_117627354insGGATA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117627353_117627354insGGATA , CM000669.2:g.117627353_117627354insGGATA	GRCh38
NC_000007.13:g.117267407_117267408insGGATA , CM000669.1:g.117267407_117267408insGGATA	GRCh37
NC_000007.12:g.117054643_117054644insGGATA	NCBI36
NG_016465.4:g.166570_166571insGGATA , LRG_663:g.166570_166571insGGATA

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.3469-169_3469-168insGGATA	ENSP00000497673.2:n.3469-169_3469-168insGGATA
ENST00000647978.2:c.*3183-169_*3183-168insGGATA	ENSP00000497658.1:n.*3183-169_*3183-168insGGATA
ENST00000649781.2:c.3286-169_3286-168insGGATA	ENSP00000497203.1:n.3286-169_3286-168insGGATA
ENST00000685018.2:c.3469-169_3469-168insGGATA	ENSP00000510194.2:n.3469-169_3469-168insGGATA
ENST00000687278.2:c.*122-169_*122-168insGGATA	ENSP00000509593.2:n.*122-169_*122-168insGGATA
ENST00000699585.1:c.3469-169_3469-168insGGATA	ENSP00000514456.1:n.3469-169_3469-168insGGATA
ENST00000699598.1:c.3469-169_3469-168insGGATA	ENSP00000514467.1:n.3469-169_3469-168insGGATA
ENST00000699599.1:c.3469-169_3469-168insGGATA	ENSP00000514468.1:n.3469-169_3469-168insGGATA
ENST00000699600.1:c.*130-169_*130-168insGGATA	ENSP00000514469.1:n.*130-169_*130-168insGGATA
ENST00000699601.1:c.*1844-169_*1844-168insGGATA	ENSP00000514470.1:n.*1844-169_*1844-168insGGATA
ENST00000699602.1:c.3463-169_3463-168insGGATA	ENSP00000514471.1:n.3463-169_3463-168insGGATA
ENST00000699604.1:c.*3293-169_*3293-168insGGATA	ENSP00000514472.1:n.*3293-169_*3293-168insGGATA
ENST00000699605.1:c.3043-169_3043-168insGGATA	ENSP00000514473.1:n.3043-169_3043-168insGGATA
ENST00000685018.1:c.217-169_217-168insGGATA	ENSP00000510194.1:n.217-169_217-168insGGATA
ENST00000687278.1:c.1256-169_1256-168insGGATA	ENSP00000509593.1:n.1256-169_1256-168insGGATA
ENST00000689011.1:c.51-169_51-168insGGATA
ENST00000003084.11:c.3469-169_3469-168insGGATA MANE Select	ENSP00000003084.6:n.3469-169_3469-168insGGATA
ENST00000647720.1:c.1119-169_1119-168insGGATA
ENST00000648260.1:c.2251-169_2251-168insGGATA	ENSP00000497957.1:n.2251-169_2251-168insGGATA
ENST00000649406.1:c.3286-169_3286-168insGGATA	ENSP00000497965.1:n.3286-169_3286-168insGGATA
ENST00000649781.1:c.3286-169_3286-168insGGATA	ENSP00000497203.1:n.3286-169_3286-168insGGATA
ENST00000003084.10:c.3469-169_3469-168insGGATA	ENSP00000003084.6:n.3469-169_3469-168insGGATA
ENST00000426809.5:c.3379-169_3379-168insGGATA	ENSP00000389119.1:n.3379-169_3379-168insGGATA
ENST00000468795.1:c.294-169_294-168insGGATA
NM_000492.3:c.3469-169_3469-168insGGATA , LRG_663t1:c.3469-169_3469-168insGGATA	NP_000483.3:n.3469-169_3469-168insGGATA
XM_011515751.1:c.3559-169_3559-168insGGATA	XP_011514053.1:n.3559-169_3559-168insGGATA
XM_011515752.1:c.3559-169_3559-168insGGATA	XP_011514054.1:n.3559-169_3559-168insGGATA
XM_011515753.1:c.3226-169_3226-168insGGATA	XP_011514055.1:n.3226-169_3226-168insGGATA
XM_011515754.1:c.3226-169_3226-168insGGATA	XP_011514056.1:n.3226-169_3226-168insGGATA
NM_000492.4:c.3469-169_3469-168insGGATA MANE Select	NP_000483.3:n.3469-169_3469-168insGGATA