Canonical Allele Identifier: CA2725065488

Gene: KMT2A

Linked Data

• dbSNP Id: rs2134392876

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503454_118503455insTTACATGGTCGTTGGCC , CM000673.2:g.118503454_118503455insTTACATGGTCGTTGGCC	GRCh38
NC_000011.9:g.118374169_118374170insTTACATGGTCGTTGGCC , CM000673.1:g.118374169_118374170insTTACATGGTCGTTGGCC	GRCh37
NC_000011.8:g.117879379_117879380insTTACATGGTCGTTGGCC	NCBI36
NG_027813.1:g.71965_71966insTTACATGGTCGTTGGCC , LRG_613:g.71965_71966insTTACATGGTCGTTGGCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.7661_7662insTTACATGGTCGTTGGCC	ENSP00000432391.3:p.Thr2555TyrfsTer10
ENST00000710560.1:c.7652_7653insTTACATGGTCGTTGGCC	ENSP00000518343.1:p.Thr2552TyrfsTer10
ENST00000649878.2:c.1601_1602insTTACATGGTCGTTGGCC	ENSP00000497891.2:p.Thr535TyrfsTer10
ENST00000685397.1:c.1601_1602insTTACATGGTCGTTGGCC	ENSP00000509586.1:p.Thr535TyrfsTer10
ENST00000686370.1:c.1601_1602insTTACATGGTCGTTGGCC	ENSP00000509179.1:p.Thr535TyrfsTer10
ENST00000689424.1:c.1859_1860insTTACATGGTCGTTGGCC	ENSP00000509852.1:p.Thr621TyrfsTer10
ENST00000691053.1:c.7634_7635insTTACATGGTCGTTGGCC	ENSP00000509168.1:p.Thr2546TyrfsTer10
ENST00000389506.10:c.7553_7554insTTACATGGTCGTTGGCC	ENSP00000374157.5:p.Thr2519TyrfsTer10
ENST00000528278.2:n.6904_6905insTTACATGGTCGTTGGCC
ENST00000534358.8:c.7562_7563insTTACATGGTCGTTGGCC MANE Select	ENSP00000436786.2:p.Thr2522TyrfsTer10
ENST00000649699.1:c.7439_7440insTTACATGGTCGTTGGCC	ENSP00000496927.1:p.Thr2481TyrfsTer10
ENST00000389506.9:c.7553_7554insTTACATGGTCGTTGGCC	ENSP00000374157.5:p.Thr2519TyrfsTer10
ENST00000528278.1:n.1689_1690insTTACATGGTCGTTGGCC
ENST00000534358.5:c.7562_7563insTTACATGGTCGTTGGCC	ENSP00000436786.1:p.Thr2522TyrfsTer10
NM_001197104.1:c.7562_7563insTTACATGGTCGTTGGCC , LRG_613t1:c.7562_7563insTTACATGGTCGTTGGCC	NP_001184033.1:p.Thr2522TyrfsTer10
NM_005933.3:c.7553_7554insTTACATGGTCGTTGGCC	NP_005924.2:p.Thr2519TyrfsTer10
XM_006718839.2:c.5045_5046insTTACATGGTCGTTGGCC	XP_006718902.2:p.Thr1683TyrfsTer10
XM_011542829.1:c.7661_7662insTTACATGGTCGTTGGCC	XP_011541131.1:p.Thr2555TyrfsTer10
XM_011542830.1:c.7658_7659insTTACATGGTCGTTGGCC	XP_011541132.1:p.Thr2554TyrfsTer10
XM_011542831.1:c.7652_7653insTTACATGGTCGTTGGCC	XP_011541133.1:p.Thr2552TyrfsTer10
XM_011542832.1:c.5468_5469insTTACATGGTCGTTGGCC	XP_011541134.1:p.Thr1824TyrfsTer10
XM_011542833.1:c.5144_5145insTTACATGGTCGTTGGCC	XP_011541135.1:p.Thr1716TyrfsTer10
XM_006718839.3:c.5045_5046insTTACATGGTCGTTGGCC	XP_006718902.2:p.Thr1683TyrfsTer10
XM_011542829.2:c.7661_7662insTTACATGGTCGTTGGCC	XP_011541131.1:p.Thr2555TyrfsTer10
XM_011542830.2:c.7658_7659insTTACATGGTCGTTGGCC	XP_011541132.1:p.Thr2554TyrfsTer10
XM_011542831.2:c.7652_7653insTTACATGGTCGTTGGCC	XP_011541133.1:p.Thr2552TyrfsTer10
XM_011542833.2:c.5144_5145insTTACATGGTCGTTGGCC	XP_011541135.1:p.Thr1716TyrfsTer10
NM_001197104.2:c.7562_7563insTTACATGGTCGTTGGCC MANE Select	NP_001184033.1:p.Thr2522TyrfsTer10
NM_005933.4:c.7553_7554insTTACATGGTCGTTGGCC	NP_005924.2:p.Thr2519TyrfsTer10