Canonical Allele Identifier: CA2725034740

Gene: KMT2A

Linked Data

• dbSNP Id: rs2134294063

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118480262_118480263insATTGTAGATTCTGACATTTT , CM000673.2:g.118480262_118480263insATTGTAGATTCTGACATTTT	GRCh38
NC_000011.9:g.118350977_118350978insATTGTAGATTCTGACATTTT , CM000673.1:g.118350977_118350978insATTGTAGATTCTGACATTTT	GRCh37
NC_000011.8:g.117856187_117856188insATTGTAGATTCTGACATTTT	NCBI36
NG_027813.1:g.48773_48774insATTGTAGATTCTGACATTTT , LRG_613:g.48773_48774insATTGTAGATTCTGACATTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.3733+24_3733+25insATTGTAGATTCTGACATTTT	ENSP00000432391.3:n.3733+24_3733+25insATTGTAGATTCTGACATTTT
ENST00000710560.1:c.3733+24_3733+25insATTGTAGATTCTGACATTTT	ENSP00000518343.1:n.3733+24_3733+25insATTGTAGATTCTGACATTTT
ENST00000527869.7:c.1216+24_1216+25insATTGTAGATTCTGACATTTT	ENSP00000432652.3:n.1216+24_1216+25insATTGTAGATTCTGACATTTT
ENST00000533790.3:c.1117+24_1117+25insATTGTAGATTCTGACATTTT	ENSP00000436700.3:n.1117+24_1117+25insATTGTAGATTCTGACATTTT
ENST00000649690.2:c.1441+24_1441+25insATTGTAGATTCTGACATTTT	ENSP00000497372.2:n.1441+24_1441+25insATTGTAGATTCTGACATTTT
ENST00000685719.1:c.615+24_615+25insATTGTAGATTCTGACATTTT
ENST00000691053.1:c.3634+24_3634+25insATTGTAGATTCTGACATTTT	ENSP00000509168.1:n.3634+24_3634+25insATTGTAGATTCTGACATTTT
ENST00000389506.10:c.3634+24_3634+25insATTGTAGATTCTGACATTTT	ENSP00000374157.5:n.3634+24_3634+25insATTGTAGATTCTGACATTTT
ENST00000533790.2:c.886+24_886+25insATTGTAGATTCTGACATTTT	ENSP00000436700.2:n.886+24_886+25insATTGTAGATTCTGACATTTT
ENST00000534358.8:c.3634+24_3634+25insATTGTAGATTCTGACATTTT MANE Select	ENSP00000436786.2:n.3634+24_3634+25insATTGTAGATTCTGACATTTT
ENST00000648261.1:c.2404+24_2404+25insATTGTAGATTCTGACATTTT	ENSP00000498126.1:n.2404+24_2404+25insATTGTAGATTCTGACATTTT
ENST00000649699.1:c.3634+24_3634+25insATTGTAGATTCTGACATTTT	ENSP00000496927.1:n.3634+24_3634+25insATTGTAGATTCTGACATTTT
ENST00000389506.9:c.3634+24_3634+25insATTGTAGATTCTGACATTTT	ENSP00000374157.5:n.3634+24_3634+25insATTGTAGATTCTGACATTTT
ENST00000531904.6:c.3733+24_3733+25insATTGTAGATTCTGACATTTT	ENSP00000432391.2:n.3733+24_3733+25insATTGTAGATTCTGACATTTT
ENST00000534358.5:c.3634+24_3634+25insATTGTAGATTCTGACATTTT	ENSP00000436786.1:n.3634+24_3634+25insATTGTAGATTCTGACATTTT
NM_001197104.1:c.3634+24_3634+25insATTGTAGATTCTGACATTTT , LRG_613t1:c.3634+24_3634+25insATTGTAGATTCTGACATTTT	NP_001184033.1:n.3634+24_3634+25insATTGTAGATTCTGACATTTT
NM_005933.3:c.3634+24_3634+25insATTGTAGATTCTGACATTTT	NP_005924.2:n.3634+24_3634+25insATTGTAGATTCTGACATTTT
XM_006718839.2:c.1117+24_1117+25insATTGTAGATTCTGACATTTT	XP_006718902.2:n.1117+24_1117+25insATTGTAGATTCTGACATTTT
XM_011542829.1:c.3733+24_3733+25insATTGTAGATTCTGACATTTT	XP_011541131.1:n.3733+24_3733+25insATTGTAGATTCTGACATTTT
XM_011542830.1:c.3733+24_3733+25insATTGTAGATTCTGACATTTT	XP_011541132.1:n.3733+24_3733+25insATTGTAGATTCTGACATTTT
XM_011542831.1:c.3733+24_3733+25insATTGTAGATTCTGACATTTT	XP_011541133.1:n.3733+24_3733+25insATTGTAGATTCTGACATTTT
XM_011542832.1:c.1540+24_1540+25insATTGTAGATTCTGACATTTT	XP_011541134.1:n.1540+24_1540+25insATTGTAGATTCTGACATTTT
XM_011542833.1:c.1216+24_1216+25insATTGTAGATTCTGACATTTT	XP_011541135.1:n.1216+24_1216+25insATTGTAGATTCTGACATTTT
XM_006718839.3:c.1117+24_1117+25insATTGTAGATTCTGACATTTT	XP_006718902.2:n.1117+24_1117+25insATTGTAGATTCTGACATTTT
XM_011542829.2:c.3733+24_3733+25insATTGTAGATTCTGACATTTT	XP_011541131.1:n.3733+24_3733+25insATTGTAGATTCTGACATTTT
XM_011542830.2:c.3733+24_3733+25insATTGTAGATTCTGACATTTT	XP_011541132.1:n.3733+24_3733+25insATTGTAGATTCTGACATTTT
XM_011542831.2:c.3733+24_3733+25insATTGTAGATTCTGACATTTT	XP_011541133.1:n.3733+24_3733+25insATTGTAGATTCTGACATTTT
XM_011542833.2:c.1216+24_1216+25insATTGTAGATTCTGACATTTT	XP_011541135.1:n.1216+24_1216+25insATTGTAGATTCTGACATTTT
NM_001197104.2:c.3634+24_3634+25insATTGTAGATTCTGACATTTT MANE Select	NP_001184033.1:n.3634+24_3634+25insATTGTAGATTCTGACATTTT
NM_005933.4:c.3634+24_3634+25insATTGTAGATTCTGACATTTT	NP_005924.2:n.3634+24_3634+25insATTGTAGATTCTGACATTTT