Canonical Allele Identifier: CA2255614987

Gene: NF1

Linked Data

• dbSNP Id: rs2070295049

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31357247T>C , CM000679.2:g.31357247T>C	GRCh38
NC_000017.10:g.29684265T>C , CM000679.1:g.29684265T>C	GRCh37
NC_000017.9:g.26708391T>C	NCBI36
NG_009018.1:g.267271T>C , LRG_214:g.267271T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7852-22T>C	ENSP00000512431.1:n.7852-22T>C
ENST00000684826.1:c.2434-22T>C	ENSP00000509994.1:n.2434-22T>C
ENST00000687027.1:c.2026-22T>C	ENSP00000508715.1:n.2026-22T>C
ENST00000687863.1:n.4515-22T>C
ENST00000689464.1:c.920-22T>C
ENST00000691014.1:c.7900-22T>C	ENSP00000510595.1:n.7900-22T>C
ENST00000693617.1:c.2434-22T>C	ENSP00000510031.1:n.2434-22T>C
ENST00000358273.9:c.7870-22T>C MANE Select	ENSP00000351015.4:n.7870-22T>C
ENST00000356175.7:c.7807-22T>C	ENSP00000348498.3:n.7807-22T>C
ENST00000358273.8:c.7870-22T>C	ENSP00000351015.4:n.7870-22T>C
ENST00000456735.6:c.6805-22T>C	ENSP00000389907.2:n.6805-22T>C
ENST00000471572.6:c.1253-22T>C
ENST00000577967.1:n.1444T>C
ENST00000579081.5:c.8006-22T>C	ENSP00000462408.1:n.8006-22T>C
ENST00000581790.5:c.855-22T>C
NM_000267.3:c.7807-22T>C , LRG_214t1:c.7807-22T>C	NP_000258.1:n.7807-22T>C
NM_001042492.2:c.7870-22T>C , LRG_214t2:c.7870-22T>C	NP_001035957.1:n.7870-22T>C
XM_005257983.1:c.7870-22T>C	XP_005258040.1:n.7870-22T>C
XM_005257984.1:c.7807-22T>C	XP_005258041.1:n.7807-22T>C
XM_006721922.1:c.7900-22T>C	XP_006721985.1:n.7900-22T>C
XM_006721923.2:c.7861-22T>C	XP_006721986.1:n.7861-22T>C
XM_006721924.1:c.7900-22T>C	XP_006721987.1:n.7900-22T>C
XM_006721925.1:c.7837-22T>C	XP_006721988.1:n.7837-22T>C
XM_006721926.2:c.7900-22T>C	XP_006721989.1:n.7900-22T>C
XM_006721927.1:c.7900-22T>C	XP_006721990.1:n.7900-22T>C
XM_011524852.1:c.7897-22T>C	XP_011523154.1:n.7897-22T>C
XM_011524853.1:c.7861-22T>C	XP_011523155.1:n.7861-22T>C
XM_011524854.1:c.7861-22T>C	XP_011523156.1:n.7861-22T>C
XM_011524855.1:c.7861-22T>C	XP_011523157.1:n.7861-22T>C
XM_011524856.1:c.7861-22T>C	XP_011523158.1:n.7861-22T>C
XM_011524857.1:c.7777-22T>C	XP_011523159.1:n.7777-22T>C
NM_001042492.3:c.7870-22T>C MANE Select	NP_001035957.1:n.7870-22T>C