Canonical Allele Identifier: CA2637086162

Gene: NF1

Linked Data

• gnomAD v4: 17-31357231-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.31357236del , CM000679.2:g.31357236del	GRCh38
NC_000017.10:g.29684254del , CM000679.1:g.29684254del	GRCh37
NC_000017.9:g.26708380del	NCBI36
NG_009018.1:g.267260del , LRG_214:g.267260del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696138.1:c.7852-33del	ENSP00000512431.1:n.7852-33del
ENST00000684826.1:c.2434-33del	ENSP00000509994.1:n.2434-33del
ENST00000687027.1:c.2026-33del	ENSP00000508715.1:n.2026-33del
ENST00000687863.1:n.4515-33del
ENST00000689464.1:c.920-33del
ENST00000691014.1:c.7900-33del	ENSP00000510595.1:n.7900-33del
ENST00000693617.1:c.2434-33del	ENSP00000510031.1:n.2434-33del
ENST00000358273.9:c.7870-33del MANE Select	ENSP00000351015.4:n.7870-33del
ENST00000356175.7:c.7807-33del	ENSP00000348498.3:n.7807-33del
ENST00000358273.8:c.7870-33del	ENSP00000351015.4:n.7870-33del
ENST00000456735.6:c.6805-33del	ENSP00000389907.2:n.6805-33del
ENST00000471572.6:c.1253-33del
ENST00000577967.1:n.1433del
ENST00000579081.5:c.8006-33del	ENSP00000462408.1:n.8006-33del
ENST00000581790.5:c.855-33del
NM_000267.3:c.7807-33del , LRG_214t1:c.7807-33del	NP_000258.1:n.7807-33del
NM_001042492.2:c.7870-33del , LRG_214t2:c.7870-33del	NP_001035957.1:n.7870-33del
XM_005257983.1:c.7870-33del	XP_005258040.1:n.7870-33del
XM_005257984.1:c.7807-33del	XP_005258041.1:n.7807-33del
XM_006721922.1:c.7900-33del	XP_006721985.1:n.7900-33del
XM_006721923.2:c.7861-33del	XP_006721986.1:n.7861-33del
XM_006721924.1:c.7900-33del	XP_006721987.1:n.7900-33del
XM_006721925.1:c.7837-33del	XP_006721988.1:n.7837-33del
XM_006721926.2:c.7900-33del	XP_006721989.1:n.7900-33del
XM_006721927.1:c.7900-33del	XP_006721990.1:n.7900-33del
XM_011524852.1:c.7897-33del	XP_011523154.1:n.7897-33del
XM_011524853.1:c.7861-33del	XP_011523155.1:n.7861-33del
XM_011524854.1:c.7861-33del	XP_011523156.1:n.7861-33del
XM_011524855.1:c.7861-33del	XP_011523157.1:n.7861-33del
XM_011524856.1:c.7861-33del	XP_011523158.1:n.7861-33del
XM_011524857.1:c.7777-33del	XP_011523159.1:n.7777-33del
NM_001042492.3:c.7870-33del MANE Select	NP_001035957.1:n.7870-33del