Canonical Allele Identifier: CA15641144
Gene: MLLT10 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21626690T>A , CM000672.2:g.21626690T>A GRCh38
NC_000010.10:g.21915619T>A , CM000672.1:g.21915619T>A GRCh37
NC_000010.9:g.21955625T>A NCBI36
NG_027818.1:g.97519T>A
NG_027818.2:g.97519T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307729.12:c.699+9483T>A MANE Select ENSP00000307411.7:n.699+9483T>A
ENST00000377072.8:c.699+9483T>A ENSP00000366272.3:n.699+9483T>A
ENST00000438473.6:c.74+9483T>A
ENST00000650893.1:c.*582+9483T>A ENSP00000499068.1:n.*582+9483T>A
ENST00000650921.1:n.83+1941T>A
ENST00000651298.1:c.*582+9483T>A ENSP00000498270.1:n.*582+9483T>A
ENST00000651382.1:n.1611+9483T>A
ENST00000651405.1:n.59+1941T>A
ENST00000652258.1:c.446+9483T>A
ENST00000307729.11:c.699+9483T>A ENSP00000307411.7:n.699+9483T>A
ENST00000377059.7:c.699+9483T>A ENSP00000366258.4:n.699+9483T>A
ENST00000377072.7:c.699+9483T>A ENSP00000366272.3:n.699+9483T>A
ENST00000631589.1:c.699+9483T>A ENSP00000488569.1:n.699+9483T>A
NM_001195626.1:c.699+9483T>A NP_001182555.1:n.699+9483T>A
NM_004641.3:c.699+9483T>A NP_004632.1:n.699+9483T>A
XM_005252605.2:c.699+9483T>A XP_005252662.1:n.699+9483T>A
XM_005252608.2:c.699+9483T>A XP_005252665.1:n.699+9483T>A
XM_005252609.2:c.699+9483T>A XP_005252666.1:n.699+9483T>A
XM_011519696.1:c.699+9483T>A XP_011517998.1:n.699+9483T>A
XM_011519697.1:c.699+9483T>A XP_011517999.1:n.699+9483T>A
XM_011519698.1:c.699+9483T>A XP_011518000.1:n.699+9483T>A
XM_011519699.1:c.699+9483T>A XP_011518001.1:n.699+9483T>A
XM_011519700.1:c.699+9483T>A XP_011518002.1:n.699+9483T>A
XM_011519701.1:c.603+11766T>A XP_011518003.1:n.603+11766T>A
XM_011519702.1:c.699+9483T>A XP_011518004.1:n.699+9483T>A
XM_011519703.1:c.465+9483T>A XP_011518005.1:n.465+9483T>A
XM_011519704.1:c.465+9483T>A XP_011518006.1:n.465+9483T>A
XM_011519705.1:c.342+9483T>A XP_011518007.1:n.342+9483T>A
XM_011519706.1:c.339+1941T>A XP_011518008.1:n.339+1941T>A
XR_930517.1:n.870+9483T>A
NM_001324297.1:c.-173+9483T>A NP_001311226.1:n.-173+9483T>A
NR_136736.1:n.1226+9483T>A
XM_024448179.1:c.699+9483T>A XP_024303947.1:n.699+9483T>A
XM_024448180.1:c.699+9483T>A XP_024303948.1:n.699+9483T>A
XM_024448181.1:c.699+9483T>A XP_024303949.1:n.699+9483T>A
XM_024448182.1:c.699+9483T>A XP_024303950.1:n.699+9483T>A
XM_024448183.1:c.699+9483T>A XP_024303951.1:n.699+9483T>A
XM_024448184.1:c.699+9483T>A XP_024303952.1:n.699+9483T>A
XM_024448186.1:c.699+9483T>A XP_024303954.1:n.699+9483T>A
XM_024448187.1:c.603+11766T>A XP_024303955.1:n.603+11766T>A
XM_024448188.1:c.603+11766T>A XP_024303956.1:n.603+11766T>A
XM_024448189.1:c.699+9483T>A XP_024303957.1:n.699+9483T>A
XM_024448190.1:c.699+9483T>A XP_024303958.1:n.699+9483T>A
XM_024448191.1:c.699+9483T>A XP_024303959.1:n.699+9483T>A
XM_024448192.1:c.465+9483T>A XP_024303960.1:n.465+9483T>A
XM_024448193.1:c.465+9483T>A XP_024303961.1:n.465+9483T>A
XM_024448194.1:c.342+9483T>A XP_024303962.1:n.342+9483T>A
XM_024448195.1:c.342+9483T>A XP_024303963.1:n.342+9483T>A
XM_024448197.1:c.342+9483T>A XP_024303965.1:n.342+9483T>A
XM_024448198.1:c.342+9483T>A XP_024303966.1:n.342+9483T>A
XM_024448199.1:c.342+9483T>A XP_024303967.1:n.342+9483T>A
XM_024448200.1:c.342+9483T>A XP_024303968.1:n.342+9483T>A
XM_024448201.1:c.339+1941T>A XP_024303969.1:n.339+1941T>A
XM_024448202.1:c.342+9483T>A XP_024303970.1:n.342+9483T>A
XM_024448204.1:c.-173+9483T>A XP_024303972.1:n.-173+9483T>A
XM_024448205.1:c.-173+9483T>A XP_024303973.1:n.-173+9483T>A
XM_024448206.1:c.699+9483T>A XP_024303974.1:n.699+9483T>A
XR_002957016.1:n.870+9483T>A
NM_001195626.3:c.699+9483T>A MANE Select NP_001182555.1:n.699+9483T>A
NM_001324297.2:c.-173+9483T>A NP_001311226.1:n.-173+9483T>A
NM_004641.4:c.699+9483T>A NP_004632.1:n.699+9483T>A
NR_136736.2:n.1166+9483T>A
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