Canonical Allele Identifier: CA2255550849

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31201525_31201529delinsTTTTC , CM000679.2:g.31201525_31201529delinsTTTTC	GRCh38
NC_000017.10:g.29528543_29528547delinsTTTTC , CM000679.1:g.29528543_29528547delinsTTTTC	GRCh37
NC_000017.9:g.26552669_26552673delinsTTTTC	NCBI36
NG_009018.1:g.111549_111553delinsTTTTC , LRG_214:g.111549_111553delinsTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.1260+40_1260+44delinsTTTTC	ENSP00000512431.1:n.1260+40_1260+44delinsTTTTC
ENST00000686189.1:c.675+40_675+44delinsTTTTC	ENSP00000509682.1:n.675+40_675+44delinsTTTTC
ENST00000688507.1:n.1006_1010delinsTTTTC
ENST00000691014.1:c.1260+40_1260+44delinsTTTTC	ENSP00000510595.1:n.1260+40_1260+44delinsTTTTC
ENST00000692326.1:n.1583_1587delinsTTTTC
ENST00000358273.9:c.1260+40_1260+44delinsTTTTC MANE Select	ENSP00000351015.4:n.1260+40_1260+44delinsTTTTC
ENST00000356175.7:c.1260+40_1260+44delinsTTTTC	ENSP00000348498.3:n.1260+40_1260+44delinsTTTTC
ENST00000358273.8:c.1260+40_1260+44delinsTTTTC	ENSP00000351015.4:n.1260+40_1260+44delinsTTTTC
ENST00000431387.8:c.1260+40_1260+44delinsTTTTC	ENSP00000412921.4:n.1260+40_1260+44delinsTTTTC
ENST00000456735.6:c.258+40_258+44delinsTTTTC	ENSP00000389907.2:n.258+40_258+44delinsTTTTC
ENST00000487476.5:n.1643+40_1643+44delinsTTTTC
ENST00000495910.6:c.1035+40_1035+44delinsTTTTC
ENST00000579081.5:c.1362+40_1362+44delinsTTTTC	ENSP00000462408.1:n.1362+40_1362+44delinsTTTTC
NM_000267.3:c.1260+40_1260+44delinsTTTTC , LRG_214t1:c.1260+40_1260+44delinsTTTTC	NP_000258.1:n.1260+40_1260+44delinsTTTTC
NM_001042492.2:c.1260+40_1260+44delinsTTTTC , LRG_214t2:c.1260+40_1260+44delinsTTTTC	NP_001035957.1:n.1260+40_1260+44delinsTTTTC
NM_001128147.2:c.1260+40_1260+44delinsTTTTC	NP_001121619.1:n.1260+40_1260+44delinsTTTTC
XM_005257983.1:c.1260+40_1260+44delinsTTTTC	XP_005258040.1:n.1260+40_1260+44delinsTTTTC
XM_005257984.1:c.1260+40_1260+44delinsTTTTC	XP_005258041.1:n.1260+40_1260+44delinsTTTTC
XM_006721922.1:c.1260+40_1260+44delinsTTTTC	XP_006721985.1:n.1260+40_1260+44delinsTTTTC
XM_006721923.2:c.1221+40_1221+44delinsTTTTC	XP_006721986.1:n.1221+40_1221+44delinsTTTTC
XM_006721924.1:c.1260+40_1260+44delinsTTTTC	XP_006721987.1:n.1260+40_1260+44delinsTTTTC
XM_006721925.1:c.1260+40_1260+44delinsTTTTC	XP_006721988.1:n.1260+40_1260+44delinsTTTTC
XM_006721926.2:c.1260+40_1260+44delinsTTTTC	XP_006721989.1:n.1260+40_1260+44delinsTTTTC
XM_006721927.1:c.1260+40_1260+44delinsTTTTC	XP_006721990.1:n.1260+40_1260+44delinsTTTTC
XM_006721928.2:c.1260+40_1260+44delinsTTTTC	XP_006721991.1:n.1260+40_1260+44delinsTTTTC
XM_011524852.1:c.1260+40_1260+44delinsTTTTC	XP_011523154.1:n.1260+40_1260+44delinsTTTTC
XM_011524853.1:c.1221+40_1221+44delinsTTTTC	XP_011523155.1:n.1221+40_1221+44delinsTTTTC
XM_011524854.1:c.1221+40_1221+44delinsTTTTC	XP_011523156.1:n.1221+40_1221+44delinsTTTTC
XM_011524855.1:c.1221+40_1221+44delinsTTTTC	XP_011523157.1:n.1221+40_1221+44delinsTTTTC
XM_011524856.1:c.1221+40_1221+44delinsTTTTC	XP_011523158.1:n.1221+40_1221+44delinsTTTTC
XM_011524857.1:c.1260+40_1260+44delinsTTTTC	XP_011523159.1:n.1260+40_1260+44delinsTTTTC
NM_001042492.3:c.1260+40_1260+44delinsTTTTC MANE Select	NP_001035957.1:n.1260+40_1260+44delinsTTTTC
NM_001128147.3:c.1260+40_1260+44delinsTTTTC	NP_001121619.1:n.1260+40_1260+44delinsTTTTC