Canonical Allele Identifier: CA2695225173

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31338704del , CM000679.2:g.31338704del	GRCh38
NC_000017.10:g.29665722del , CM000679.1:g.29665722del	GRCh37
NC_000017.9:g.26689848del	NCBI36
NG_009018.1:g.248728del , LRG_214:g.248728del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.6802del
ENST00000684826.1:c.1384del
ENST00000684998.1:n.2642del
ENST00000687027.1:c.976del
ENST00000687863.1:n.3465del
ENST00000691014.1:c.6850del
ENST00000693617.1:c.1384del
ENST00000358273.9:c.6820del
ENST00000356175.7:c.6757del
ENST00000358273.8:c.6820del
ENST00000456735.6:c.5755del
ENST00000471572.6:c.203del
ENST00000579081.5:c.6956del
ENST00000581790.5:c.64+824del
ENST00000584328.1:n.234del
NM_000267.3:c.6757del , LRG_214t1:c.6757del
NM_001042492.2:c.6820del , LRG_214t2:c.6820del
XM_005257983.1:c.6820del
XM_005257984.1:c.6757del
XM_006721922.1:c.6850del
XM_006721923.2:c.6811del
XM_006721924.1:c.6850del
XM_006721925.1:c.6787del
XM_006721926.2:c.6850del
XM_006721927.1:c.6850del
XM_011524852.1:c.6847del
XM_011524853.1:c.6811del
XM_011524854.1:c.6811del
XM_011524855.1:c.6811del
XM_011524856.1:c.6811del
XM_011524857.1:c.6850del
NM_001042492.3:c.6820del