Canonical Allele Identifier: CA2637073155

Gene: NF1

Linked Data

• gnomAD v4: 17-31155839-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31155839A>T , CM000679.2:g.31155839A>T	GRCh38
NC_000017.10:g.29482857A>T , CM000679.1:g.29482857A>T	GRCh37
NC_000017.9:g.26506983A>T	NCBI36
NG_009018.1:g.65863A>T , LRG_214:g.65863A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.61-144A>T	ENSP00000512431.1:n.61-144A>T
ENST00000691014.1:c.61-144A>T	ENSP00000510595.1:n.61-144A>T
ENST00000358273.9:c.61-144A>T MANE Select	ENSP00000351015.4:n.61-144A>T
ENST00000356175.7:c.61-144A>T	ENSP00000348498.3:n.61-144A>T
ENST00000358273.8:c.61-144A>T	ENSP00000351015.4:n.61-144A>T
ENST00000431387.8:c.61-144A>T	ENSP00000412921.4:n.61-144A>T
ENST00000487476.5:n.444-144A>T
ENST00000489712.6:c.-141-144A>T	ENSP00000467284.1:n.-141-144A>T
ENST00000579081.5:c.163-144A>T	ENSP00000462408.1:n.163-144A>T
NM_000267.3:c.61-144A>T , LRG_214t1:c.61-144A>T	NP_000258.1:n.61-144A>T
NM_001042492.2:c.61-144A>T , LRG_214t2:c.61-144A>T	NP_001035957.1:n.61-144A>T
NM_001128147.2:c.61-144A>T	NP_001121619.1:n.61-144A>T
XM_005257983.1:c.61-144A>T	XP_005258040.1:n.61-144A>T
XM_005257984.1:c.61-144A>T	XP_005258041.1:n.61-144A>T
XM_006721922.1:c.61-144A>T	XP_006721985.1:n.61-144A>T
XM_006721923.2:c.22-144A>T	XP_006721986.1:n.22-144A>T
XM_006721924.1:c.61-144A>T	XP_006721987.1:n.61-144A>T
XM_006721925.1:c.61-144A>T	XP_006721988.1:n.61-144A>T
XM_006721926.2:c.61-144A>T	XP_006721989.1:n.61-144A>T
XM_006721927.1:c.61-144A>T	XP_006721990.1:n.61-144A>T
XM_006721928.2:c.61-144A>T	XP_006721991.1:n.61-144A>T
XM_011524852.1:c.61-144A>T	XP_011523154.1:n.61-144A>T
XM_011524853.1:c.22-144A>T	XP_011523155.1:n.22-144A>T
XM_011524854.1:c.22-144A>T	XP_011523156.1:n.22-144A>T
XM_011524855.1:c.22-144A>T	XP_011523157.1:n.22-144A>T
XM_011524856.1:c.22-144A>T	XP_011523158.1:n.22-144A>T
XM_011524857.1:c.61-144A>T	XP_011523159.1:n.61-144A>T
NM_001042492.3:c.61-144A>T MANE Select	NP_001035957.1:n.61-144A>T
NM_001128147.3:c.61-144A>T	NP_001121619.1:n.61-144A>T