Canonical Allele Identifier: CA353562016
Community Standard Title: NM_001354604.2(MITF):c.1096C>T (p.Arg366Ter)
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69959337C>T , CM000665.2:g.69959337C>T GRCh38
NC_000003.11:g.70008488C>T , CM000665.1:g.70008488C>T GRCh37
NC_000003.10:g.70091178C>T NCBI36
NG_011631.1:g.224856C>T , LRG_776:g.224856C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001354604.2:c.1096C>T MANE Select NP_001341533.1:p.Arg366Ter
ENST00000352241.9:c.1096C>T MANE Select ENSP00000295600.8:p.Arg366Ter
NM_000248.4:c.775C>T MANE Plus Clinical NP_000239.1:p.Arg259Ter
ENST00000394351.9:c.775C>T MANE Plus Clinical ENSP00000377880.3:p.Arg259Ter
NM_000248.3:c.775C>T , LRG_776t1:c.775C>T NP_000239.1:p.Arg259Ter
NM_001184967.1:c.922C>T NP_001171896.1:p.Arg308Ter
NM_001184967.2:c.922C>T NP_001171896.1:p.Arg308Ter
NM_001354604.1:c.1096C>T NP_001341533.1:p.Arg366Ter
NM_001354605.1:c.1093C>T NP_001341534.1:p.Arg365Ter
NM_001354605.2:c.1093C>T NP_001341534.1:p.Arg365Ter
NM_001354606.1:c.1075C>T NP_001341535.1:p.Arg359Ter
NM_001354606.2:c.1075C>T NP_001341535.1:p.Arg359Ter
NM_001354607.1:c.1027C>T NP_001341536.1:p.Arg343Ter
NM_001354607.2:c.1027C>T NP_001341536.1:p.Arg343Ter
NM_001354608.1:c.922C>T NP_001341537.1:p.Arg308Ter
NM_001354608.2:c.922C>T NP_001341537.1:p.Arg308Ter
NM_006722.2:c.1075C>T NP_006713.1:p.Arg359Ter
NM_006722.3:c.1075C>T NP_006713.1:p.Arg359Ter
NM_198158.2:c.757C>T NP_937801.1:p.Arg253Ter
NM_198158.3:c.757C>T NP_937801.1:p.Arg253Ter
NM_198159.2:c.1078C>T NP_937802.1:p.Arg360Ter
NM_198159.3:c.1078C>T NP_937802.1:p.Arg360Ter
NM_198177.2:c.1030C>T NP_937820.1:p.Arg344Ter
NM_198177.3:c.1030C>T NP_937820.1:p.Arg344Ter
NM_198178.2:c.589C>T NP_937821.2:p.Arg197Ter
NM_198178.3:c.589C>T NP_937821.2:p.Arg197Ter
ENST00000314557.10:c.757C>T ENSP00000324246.6:p.Arg253Ter
ENST00000314589.10:c.1030C>T ENSP00000324443.5:p.Arg344Ter
ENST00000314589.11:c.1030C>T ENSP00000324443.5:p.Arg344Ter
ENST00000314589.9:c.1030C>T ENSP00000324443.5:p.Arg344Ter
ENST00000328528.10:c.1075C>T ENSP00000327867.6:p.Arg359Ter
ENST00000352241.8:c.1078C>T ENSP00000295600.7:p.Arg360Ter
ENST00000394351.7:c.775C>T ENSP00000377880.3:p.Arg259Ter
ENST00000448226.6:c.1096C>T ENSP00000391803.2:p.Arg366Ter
ENST00000448226.9:c.1075C>T ENSP00000391803.3:p.Arg359Ter
ENST00000451708.5:c.1048C>T ENSP00000398639.1:p.Arg350Ter
ENST00000472437.5:c.922C>T ENSP00000418845.1:p.Arg308Ter
ENST00000478490.5:c.*422C>T ENSP00000433487.1:n.*422C>T
ENST00000531774.1:c.589C>T ENSP00000435909.1:p.Arg197Ter
ENST00000642352.1:c.1078C>T ENSP00000494105.1:p.Arg360Ter
ENST00000687384.1:c.1027C>T ENSP00000510225.1:p.Arg343Ter
ENST00000689390.1:n.1252C>T
ENST00000693031.1:c.1003C>T ENSP00000509845.1:p.Arg335Ter
ENST00000693549.1:c.1030C>T ENSP00000509358.1:p.Arg344Ter
XM_005264754.1:c.1096C>T XP_005264811.1:p.Arg366Ter
XM_005264755.2:c.1048C>T XP_005264812.1:p.Arg350Ter
XM_006713164.2:c.940C>T XP_006713227.1:p.Arg314Ter
XM_011533722.1:c.1093C>T XP_011532024.1:p.Arg365Ter
XM_011533723.1:c.1045C>T XP_011532025.1:p.Arg349Ter
XM_011533724.1:c.940C>T XP_011532026.1:p.Arg314Ter
XM_011533725.1:c.928C>T XP_011532027.1:p.Arg310Ter
XM_011533726.1:c.910C>T XP_011532028.1:p.Arg304Ter