Canonical Allele Identifier: CA2684617028

Gene: CFTR

Linked Data

• gnomAD v4: 7-117480034-CTTTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.117480035_117480038del , CM000669.2:g.117480035_117480038del	GRCh38
NC_000007.13:g.117120089_117120092del , CM000669.1:g.117120089_117120092del	GRCh37
NC_000007.12:g.116907325_116907328del	NCBI36
NG_016465.4:g.19252_19255del , LRG_663:g.19252_19255del

Transcript Alleles

HGVS	Amino-acid change
ENST00000647720.2:c.-60_-57del	ENSP00000497673.2:n.-60_-57del
ENST00000647978.2:c.-60_-57del	ENSP00000497658.1:n.-60_-57del
ENST00000649781.2:c.-60_-57del	ENSP00000497203.1:n.-60_-57del
ENST00000649850.2:c.-60_-57del	ENSP00000514457.1:n.-60_-57del
ENST00000685018.2:c.-60_-57del	ENSP00000510194.2:n.-60_-57del
ENST00000687278.2:c.-60_-57del	ENSP00000509593.2:n.-60_-57del
ENST00000692802.2:n.25_28del
ENST00000693465.2:n.26_29del
ENST00000693480.2:n.25_28del
ENST00000699585.1:c.-60_-57del	ENSP00000514456.1:n.-60_-57del
ENST00000699596.1:c.-60_-57del	ENSP00000514465.1:n.-60_-57del
ENST00000699597.1:c.-60_-57del	ENSP00000514466.1:n.-60_-57del
ENST00000699598.1:c.-60_-57del	ENSP00000514467.1:n.-60_-57del
ENST00000699599.1:c.-60_-57del	ENSP00000514468.1:n.-60_-57del
ENST00000699600.1:c.-60_-57del	ENSP00000514469.1:n.-60_-57del
ENST00000699601.1:c.-60_-57del	ENSP00000514470.1:n.-60_-57del
ENST00000699602.1:c.-60_-57del	ENSP00000514471.1:n.-60_-57del
ENST00000699603.1:n.25_28del
ENST00000699604.1:c.-60_-57del	ENSP00000514472.1:n.-60_-57del
ENST00000699605.1:c.-412_-409del	ENSP00000514473.1:n.-412_-409del
ENST00000446805.2:c.-191+341_-191+344del	ENSP00000417012.1:n.-191+341_-191+344del
ENST00000692802.1:n.11_14del
ENST00000693465.1:n.11_14del
ENST00000693480.1:n.11_14del
ENST00000003084.11:c.-60_-57del MANE Select	ENSP00000003084.6:n.-60_-57del
ENST00000647639.1:n.25_28del
ENST00000647978.1:c.-60_-57del	ENSP00000497658.1:n.-60_-57del
ENST00000648260.1:c.-60_-57del	ENSP00000497957.1:n.-60_-57del
ENST00000649406.1:c.-60_-57del	ENSP00000497965.1:n.-60_-57del
ENST00000649850.1:n.24_27del
ENST00000673785.1:c.-406+14204_-406+14207del	ENSP00000501235.1:n.-406+14204_-406+14207del
ENST00000003084.10:c.-60_-57del	ENSP00000003084.6:n.-60_-57del
ENST00000446805.1:c.-191+341_-191+344del	ENSP00000417012.1:n.-191+341_-191+344del
ENST00000546407.1:n.166+4227_166+4230del
NM_000492.3:c.-60_-57del , LRG_663t1:c.-60_-57del	NP_000483.3:n.-60_-57del
XM_011515751.1:c.143+690_143+693del	XP_011514053.1:n.143+690_143+693del
XM_011515752.1:c.143+690_143+693del	XP_011514054.1:n.143+690_143+693del
XM_011515753.1:c.-191+341_-191+344del	XP_011514055.1:n.-191+341_-191+344del
XM_011515754.1:c.-518-113_-518-110del	XP_011514056.1:n.-518-113_-518-110del
NM_000492.4:c.-60_-57del MANE Select	NP_000483.3:n.-60_-57del