Canonical Allele Identifier: CA2255538675

Gene: NF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31155969_31155970delinsTC , CM000679.2:g.31155969_31155970delinsTC	GRCh38
NC_000017.10:g.29482987_29482988delinsTC , CM000679.1:g.29482987_29482988delinsTC	GRCh37
NC_000017.9:g.26507113_26507114delinsTC	NCBI36
NG_009018.1:g.65993_65994delinsTC , LRG_214:g.65993_65994delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.61-14_61-13delinsTC	ENSP00000512431.1:n.61-14_61-13delinsTC
ENST00000691014.1:c.61-14_61-13delinsTC	ENSP00000510595.1:n.61-14_61-13delinsTC
ENST00000358273.9:c.61-14_61-13delinsTC MANE Select	ENSP00000351015.4:n.61-14_61-13delinsTC
ENST00000356175.7:c.61-14_61-13delinsTC	ENSP00000348498.3:n.61-14_61-13delinsTC
ENST00000358273.8:c.61-14_61-13delinsTC	ENSP00000351015.4:n.61-14_61-13delinsTC
ENST00000431387.8:c.61-14_61-13delinsTC	ENSP00000412921.4:n.61-14_61-13delinsTC
ENST00000487476.5:n.444-14_444-13delinsTC
ENST00000489712.6:c.-141-14_-141-13delinsTC	ENSP00000467284.1:n.-141-14_-141-13delinsTC
ENST00000579081.5:c.163-14_163-13delinsTC	ENSP00000462408.1:n.163-14_163-13delinsTC
NM_000267.3:c.61-14_61-13delinsTC , LRG_214t1:c.61-14_61-13delinsTC	NP_000258.1:n.61-14_61-13delinsTC
NM_001042492.2:c.61-14_61-13delinsTC , LRG_214t2:c.61-14_61-13delinsTC	NP_001035957.1:n.61-14_61-13delinsTC
NM_001128147.2:c.61-14_61-13delinsTC	NP_001121619.1:n.61-14_61-13delinsTC
XM_005257983.1:c.61-14_61-13delinsTC	XP_005258040.1:n.61-14_61-13delinsTC
XM_005257984.1:c.61-14_61-13delinsTC	XP_005258041.1:n.61-14_61-13delinsTC
XM_006721922.1:c.61-14_61-13delinsTC	XP_006721985.1:n.61-14_61-13delinsTC
XM_006721923.2:c.22-14_22-13delinsTC	XP_006721986.1:n.22-14_22-13delinsTC
XM_006721924.1:c.61-14_61-13delinsTC	XP_006721987.1:n.61-14_61-13delinsTC
XM_006721925.1:c.61-14_61-13delinsTC	XP_006721988.1:n.61-14_61-13delinsTC
XM_006721926.2:c.61-14_61-13delinsTC	XP_006721989.1:n.61-14_61-13delinsTC
XM_006721927.1:c.61-14_61-13delinsTC	XP_006721990.1:n.61-14_61-13delinsTC
XM_006721928.2:c.61-14_61-13delinsTC	XP_006721991.1:n.61-14_61-13delinsTC
XM_011524852.1:c.61-14_61-13delinsTC	XP_011523154.1:n.61-14_61-13delinsTC
XM_011524853.1:c.22-14_22-13delinsTC	XP_011523155.1:n.22-14_22-13delinsTC
XM_011524854.1:c.22-14_22-13delinsTC	XP_011523156.1:n.22-14_22-13delinsTC
XM_011524855.1:c.22-14_22-13delinsTC	XP_011523157.1:n.22-14_22-13delinsTC
XM_011524856.1:c.22-14_22-13delinsTC	XP_011523158.1:n.22-14_22-13delinsTC
XM_011524857.1:c.61-14_61-13delinsTC	XP_011523159.1:n.61-14_61-13delinsTC
NM_001042492.3:c.61-14_61-13delinsTC MANE Select	NP_001035957.1:n.61-14_61-13delinsTC
NM_001128147.3:c.61-14_61-13delinsTC	NP_001121619.1:n.61-14_61-13delinsTC