Canonical Allele Identifier: CA2146520924
Gene: NUMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73276748T= , CM000676.2:g.73276748T= GRCh38
NC_000014.8:g.73743456T= , CM000676.1:g.73743456T= GRCh37
NC_000014.7:g.72813209T= NCBI36
NG_029061.2:g.186833A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555238.6:c.1786A= MANE Select ENSP00000451300.1:p.Arg596=
ENST00000355058.7:c.1786A= ENSP00000347169.3:p.Arg596=
ENST00000356296.8:c.1642A= ENSP00000348644.4:p.Arg548=
ENST00000359560.7:c.1753A= ENSP00000352563.3:p.Arg585=
ENST00000535282.5:c.1642A= ENSP00000441258.2:p.Arg548=
ENST00000544991.7:c.1201A= ENSP00000446001.3:p.Arg401=
ENST00000554521.6:c.1168A= ENSP00000450817.2:p.Arg390=
ENST00000554546.5:c.1609A= ENSP00000452416.1:p.Arg537=
ENST00000555238.5:c.1786A= ENSP00000451300.1:p.Arg596=
ENST00000555394.5:c.1642A= ENSP00000451625.1:p.Arg548=
ENST00000555738.6:c.1315A= ENSP00000452069.2:p.Arg439=
ENST00000556772.5:c.1354A= ENSP00000451513.1:p.Arg452=
ENST00000557597.5:c.1753A= ENSP00000451117.1:p.Arg585=
ENST00000559312.5:c.1201A= ENSP00000452888.1:p.Arg401=
ENST00000560335.5:c.1348A= ENSP00000453209.1:p.Arg450=
NM_001005743.1:c.1786A= NP_001005743.1:p.Arg596=
NM_001005744.1:c.1642A= NP_001005744.1:p.Arg548=
NM_001005745.1:c.1609A= NP_001005745.1:p.Arg537=
NM_003744.5:c.1753A= NP_003735.3:p.Arg585=
XM_005268142.3:c.1786A= XP_005268199.1:p.Arg596=
XM_005268144.3:c.1753A= XP_005268201.1:p.Arg585=
XM_005268145.3:c.1744A= XP_005268202.1:p.Arg582=
XM_005268146.3:c.1642A= XP_005268203.1:p.Arg548=
XM_011537253.1:c.1786A= XP_011535555.1:p.Arg596=
XM_011537254.1:c.1786A= XP_011535556.1:p.Arg596=
XM_011537255.1:c.1786A= XP_011535557.1:p.Arg596=
XM_011537256.1:c.1777A= XP_011535558.1:p.Arg593=
XM_011537257.1:c.1753A= XP_011535559.1:p.Arg585=
XM_011537258.1:c.1753A= XP_011535560.1:p.Arg585=
XM_011537259.1:c.1744A= XP_011535561.1:p.Arg582=
XM_011537260.1:c.1642A= XP_011535562.1:p.Arg548=
XM_011537261.1:c.1633A= XP_011535563.1:p.Arg545=
XM_011537262.1:c.1492A= XP_011535564.1:p.Arg498=
XM_011537263.1:c.1348A= XP_011535565.1:p.Arg450=
XM_011537264.1:c.1315A= XP_011535566.1:p.Arg439=
NM_001320114.1:c.1642A= NP_001307043.1:p.Arg548=
NM_001005743.2:c.1786A= MANE Select NP_001005743.1:p.Arg596=
NM_001005744.2:c.1642A= NP_001005744.1:p.Arg548=
NM_001005745.2:c.1609A= NP_001005745.1:p.Arg537=
NM_001320114.2:c.1642A= NP_001307043.1:p.Arg548=
NM_003744.6:c.1753A= NP_003735.3:p.Arg585=