Canonical Allele Identifier: CA2255603209

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31338858_31338859delinsGT , CM000679.2:g.31338858_31338859delinsGT	GRCh38
NC_000017.10:g.29665876_29665877delinsGT , CM000679.1:g.29665876_29665877delinsGT	GRCh37
NC_000017.9:g.26690002_26690003delinsGT	NCBI36
NG_009018.1:g.248882_248883delinsGT , LRG_214:g.248882_248883delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.6903+53_6903+54delinsGT	ENSP00000512431.1:n.6903+53_6903+54delinsGT
ENST00000684826.1:c.1485+53_1485+54delinsGT	ENSP00000509994.1:n.1485+53_1485+54delinsGT
ENST00000684998.1:n.2796_2797delinsGT
ENST00000687027.1:c.1077+53_1077+54delinsGT	ENSP00000508715.1:n.1077+53_1077+54delinsGT
ENST00000687863.1:n.3566+53_3566+54delinsGT
ENST00000691014.1:c.6951+53_6951+54delinsGT	ENSP00000510595.1:n.6951+53_6951+54delinsGT
ENST00000693617.1:c.1485+53_1485+54delinsGT	ENSP00000510031.1:n.1485+53_1485+54delinsGT
ENST00000358273.9:c.6921+53_6921+54delinsGT MANE Select	ENSP00000351015.4:n.6921+53_6921+54delinsGT
ENST00000356175.7:c.6858+53_6858+54delinsGT	ENSP00000348498.3:n.6858+53_6858+54delinsGT
ENST00000358273.8:c.6921+53_6921+54delinsGT	ENSP00000351015.4:n.6921+53_6921+54delinsGT
ENST00000456735.6:c.5856+53_5856+54delinsGT	ENSP00000389907.2:n.5856+53_5856+54delinsGT
ENST00000471572.6:c.304+53_304+54delinsGT
ENST00000579081.5:c.7057+53_7057+54delinsGT	ENSP00000462408.1:n.7057+53_7057+54delinsGT
ENST00000581790.5:c.64+978_64+979delinsGT
ENST00000584328.1:n.335+53_335+54delinsGT
NM_000267.3:c.6858+53_6858+54delinsGT , LRG_214t1:c.6858+53_6858+54delinsGT	NP_000258.1:n.6858+53_6858+54delinsGT
NM_001042492.2:c.6921+53_6921+54delinsGT , LRG_214t2:c.6921+53_6921+54delinsGT	NP_001035957.1:n.6921+53_6921+54delinsGT
XM_005257983.1:c.6921+53_6921+54delinsGT	XP_005258040.1:n.6921+53_6921+54delinsGT
XM_005257984.1:c.6858+53_6858+54delinsGT	XP_005258041.1:n.6858+53_6858+54delinsGT
XM_006721922.1:c.6951+53_6951+54delinsGT	XP_006721985.1:n.6951+53_6951+54delinsGT
XM_006721923.2:c.6912+53_6912+54delinsGT	XP_006721986.1:n.6912+53_6912+54delinsGT
XM_006721924.1:c.6951+53_6951+54delinsGT	XP_006721987.1:n.6951+53_6951+54delinsGT
XM_006721925.1:c.6888+53_6888+54delinsGT	XP_006721988.1:n.6888+53_6888+54delinsGT
XM_006721926.2:c.6951+53_6951+54delinsGT	XP_006721989.1:n.6951+53_6951+54delinsGT
XM_006721927.1:c.6951+53_6951+54delinsGT	XP_006721990.1:n.6951+53_6951+54delinsGT
XM_011524852.1:c.6948+53_6948+54delinsGT	XP_011523154.1:n.6948+53_6948+54delinsGT
XM_011524853.1:c.6912+53_6912+54delinsGT	XP_011523155.1:n.6912+53_6912+54delinsGT
XM_011524854.1:c.6912+53_6912+54delinsGT	XP_011523156.1:n.6912+53_6912+54delinsGT
XM_011524855.1:c.6912+53_6912+54delinsGT	XP_011523157.1:n.6912+53_6912+54delinsGT
XM_011524856.1:c.6912+53_6912+54delinsGT	XP_011523158.1:n.6912+53_6912+54delinsGT
XM_011524857.1:c.6951+53_6951+54delinsGT	XP_011523159.1:n.6951+53_6951+54delinsGT
NM_001042492.3:c.6921+53_6921+54delinsGT MANE Select	NP_001035957.1:n.6921+53_6921+54delinsGT