Canonical Allele Identifier: CA5435078

Gene: MLLT10

Linked Data

• dbSNP Id: rs142554860
• ExAC: 10:22019855 G / C
• gnomAD v2: 10-22019855-G-C
• gnomAD v4: 10-21730926-G-C
• MyVariant Identifiers: chr10:g.22019855G>C (hg19) ; chr10:g.21730926G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.21730926G>C , CM000672.2:g.21730926G>C	GRCh38
NC_000010.10:g.22019855G>C , CM000672.1:g.22019855G>C	GRCh37
NC_000010.9:g.22059861G>C	NCBI36
NG_027818.1:g.201755G>C
NG_027818.2:g.201755G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000307729.12:c.2090G>C MANE Select	ENSP00000307411.7:p.Arg697Pro
ENST00000377072.8:c.2138G>C	ENSP00000366272.3:p.Arg713Pro
ENST00000438473.6:c.1174G>C
ENST00000650893.1:c.*2109G>C	ENSP00000499068.1:n.*2109G>C
ENST00000651298.1:c.*2091G>C	ENSP00000498270.1:n.*2091G>C
ENST00000651382.1:n.3113G>C
ENST00000307729.11:c.2090G>C	ENSP00000307411.7:p.Arg697Pro
ENST00000377059.7:c.2090G>C	ENSP00000366258.4:p.Arg697Pro
ENST00000377072.7:c.2138G>C	ENSP00000366272.3:p.Arg713Pro
ENST00000438473.5:c.1067G>C	ENSP00000408281.1:p.Arg356Pro
ENST00000631589.1:c.2090G>C	ENSP00000488569.1:p.Arg697Pro
NM_001195626.1:c.2090G>C	NP_001182555.1:p.Arg697Pro
NM_004641.3:c.2138G>C	NP_004632.1:p.Arg713Pro
XM_005252605.2:c.2138G>C	XP_005252662.1:p.Arg713Pro
XM_005252608.2:c.2090G>C	XP_005252665.1:p.Arg697Pro
XM_005252609.2:c.2057G>C	XP_005252666.1:p.Arg686Pro
XM_011519696.1:c.2192G>C	XP_011517998.1:p.Arg731Pro
XM_011519697.1:c.2192G>C	XP_011517999.1:p.Arg731Pro
XM_011519698.1:c.2192G>C	XP_011518000.1:p.Arg731Pro
XM_011519699.1:c.2159G>C	XP_011518001.1:p.Arg720Pro
XM_011519700.1:c.2105G>C	XP_011518002.1:p.Arg702Pro
XM_011519701.1:c.2096G>C	XP_011518003.1:p.Arg699Pro
XM_011519702.1:c.2192G>C	XP_011518004.1:p.Arg731Pro
XM_011519703.1:c.1958G>C	XP_011518005.1:p.Arg653Pro
XM_011519704.1:c.1958G>C	XP_011518006.1:p.Arg653Pro
XM_011519705.1:c.1835G>C	XP_011518007.1:p.Arg612Pro
XM_011519706.1:c.1832G>C	XP_011518008.1:p.Arg611Pro
XM_011519707.1:c.1421G>C	XP_011518009.1:p.Arg474Pro
XR_930517.1:n.2363G>C
NM_001324297.1:c.1355G>C	NP_001311226.1:p.Arg452Pro
NR_136736.1:n.2735G>C
XM_024448179.1:c.2192G>C	XP_024303947.1:p.Arg731Pro
XM_024448180.1:c.2192G>C	XP_024303948.1:p.Arg731Pro
XM_024448181.1:c.2192G>C	XP_024303949.1:p.Arg731Pro
XM_024448182.1:c.2192G>C	XP_024303950.1:p.Arg731Pro
XM_024448183.1:c.2159G>C	XP_024303951.1:p.Arg720Pro
XM_024448184.1:c.2138G>C	XP_024303952.1:p.Arg713Pro
XM_024448186.1:c.2105G>C	XP_024303954.1:p.Arg702Pro
XM_024448187.1:c.2096G>C	XP_024303955.1:p.Arg699Pro
XM_024448188.1:c.2096G>C	XP_024303956.1:p.Arg699Pro
XM_024448189.1:c.2090G>C	XP_024303957.1:p.Arg697Pro
XM_024448190.1:c.2057G>C	XP_024303958.1:p.Arg686Pro
XM_024448191.1:c.2192G>C	XP_024303959.1:p.Arg731Pro
XM_024448192.1:c.1958G>C	XP_024303960.1:p.Arg653Pro
XM_024448193.1:c.1958G>C	XP_024303961.1:p.Arg653Pro
XM_024448194.1:c.1835G>C	XP_024303962.1:p.Arg612Pro
XM_024448195.1:c.1835G>C	XP_024303963.1:p.Arg612Pro
XM_024448197.1:c.1835G>C	XP_024303965.1:p.Arg612Pro
XM_024448198.1:c.1835G>C	XP_024303966.1:p.Arg612Pro
XM_024448199.1:c.1835G>C	XP_024303967.1:p.Arg612Pro
XM_024448200.1:c.1835G>C	XP_024303968.1:p.Arg612Pro
XM_024448201.1:c.1832G>C	XP_024303969.1:p.Arg611Pro
XM_024448202.1:c.1733G>C	XP_024303970.1:p.Arg578Pro
XM_024448203.1:c.1574G>C	XP_024303971.1:p.Arg525Pro
XM_024448204.1:c.1457G>C	XP_024303972.1:p.Arg486Pro
XM_024448205.1:c.1355G>C	XP_024303973.1:p.Arg452Pro
XR_001747388.1:n.1011-3863C>G
XR_002957016.1:n.2363G>C
NM_001195626.3:c.2090G>C MANE Select	NP_001182555.1:p.Arg697Pro
NM_001324297.2:c.1355G>C	NP_001311226.1:p.Arg452Pro
NM_004641.4:c.2138G>C	NP_004632.1:p.Arg713Pro
NR_136736.2:n.2675G>C