Canonical Allele Identifier: CA2255559602

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31222000_31222003delinsTCTG , CM000679.2:g.31222000_31222003delinsTCTG	GRCh38
NC_000017.10:g.29549018_29549021delinsTCTG , CM000679.1:g.29549018_29549021delinsTCTG	GRCh37
NC_000017.9:g.26573144_26573147delinsTCTG	NCBI36
NG_009018.1:g.132024_132027delinsTCTG , LRG_214:g.132024_132027delinsTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.1766+71_1766+74delinsTCTG	ENSP00000512431.1:n.1766+71_1766+74delinsTCTG
ENST00000686189.1:c.1237_1240delinsTCTG	ENSP00000509682.1:n.1237_1240delinsTCTG
ENST00000691014.1:c.1751+71_1751+74delinsTCTG	ENSP00000510595.1:n.1751+71_1751+74delinsTCTG
ENST00000358273.9:c.1721+71_1721+74delinsTCTG MANE Select	ENSP00000351015.4:n.1721+71_1721+74delinsTCTG
ENST00000356175.7:c.1721+71_1721+74delinsTCTG	ENSP00000348498.3:n.1721+71_1721+74delinsTCTG
ENST00000358273.8:c.1721+71_1721+74delinsTCTG	ENSP00000351015.4:n.1721+71_1721+74delinsTCTG
ENST00000431387.8:c.*10_*13delinsTCTG	ENSP00000412921.4:n.*10_*13delinsTCTG
ENST00000456735.6:c.719+71_719+74delinsTCTG	ENSP00000389907.2:n.719+71_719+74delinsTCTG
ENST00000495910.6:c.1496+71_1496+74delinsTCTG
ENST00000579081.5:c.1823+71_1823+74delinsTCTG	ENSP00000462408.1:n.1823+71_1823+74delinsTCTG
NM_000267.3:c.1721+71_1721+74delinsTCTG , LRG_214t1:c.1721+71_1721+74delinsTCTG	NP_000258.1:n.1721+71_1721+74delinsTCTG
NM_001042492.2:c.1721+71_1721+74delinsTCTG , LRG_214t2:c.1721+71_1721+74delinsTCTG	NP_001035957.1:n.1721+71_1721+74delinsTCTG
NM_001128147.2:c.*10_*13delinsTCTG	NP_001121619.1:n.*10_*13delinsTCTG
XM_005257983.1:c.1721+71_1721+74delinsTCTG	XP_005258040.1:n.1721+71_1721+74delinsTCTG
XM_005257984.1:c.1721+71_1721+74delinsTCTG	XP_005258041.1:n.1721+71_1721+74delinsTCTG
XM_006721922.1:c.1751+71_1751+74delinsTCTG	XP_006721985.1:n.1751+71_1751+74delinsTCTG
XM_006721923.2:c.1712+71_1712+74delinsTCTG	XP_006721986.1:n.1712+71_1712+74delinsTCTG
XM_006721924.1:c.1751+71_1751+74delinsTCTG	XP_006721987.1:n.1751+71_1751+74delinsTCTG
XM_006721925.1:c.1751+71_1751+74delinsTCTG	XP_006721988.1:n.1751+71_1751+74delinsTCTG
XM_006721926.2:c.1751+71_1751+74delinsTCTG	XP_006721989.1:n.1751+71_1751+74delinsTCTG
XM_006721927.1:c.1751+71_1751+74delinsTCTG	XP_006721990.1:n.1751+71_1751+74delinsTCTG
XM_006721928.2:c.1751+71_1751+74delinsTCTG	XP_006721991.1:n.1751+71_1751+74delinsTCTG
XM_011524852.1:c.1751+71_1751+74delinsTCTG	XP_011523154.1:n.1751+71_1751+74delinsTCTG
XM_011524853.1:c.1712+71_1712+74delinsTCTG	XP_011523155.1:n.1712+71_1712+74delinsTCTG
XM_011524854.1:c.1712+71_1712+74delinsTCTG	XP_011523156.1:n.1712+71_1712+74delinsTCTG
XM_011524855.1:c.1712+71_1712+74delinsTCTG	XP_011523157.1:n.1712+71_1712+74delinsTCTG
XM_011524856.1:c.1712+71_1712+74delinsTCTG	XP_011523158.1:n.1712+71_1712+74delinsTCTG
XM_011524857.1:c.1751+71_1751+74delinsTCTG	XP_011523159.1:n.1751+71_1751+74delinsTCTG
NM_001042492.3:c.1721+71_1721+74delinsTCTG MANE Select	NP_001035957.1:n.1721+71_1721+74delinsTCTG
NM_001128147.3:c.*10_*13delinsTCTG	NP_001121619.1:n.*10_*13delinsTCTG