Canonical Allele Identifier: CA942722119

Gene: KMT2A

Linked Data

• gnomAD v3: 11-118480334-G-GTTTT
• gnomAD v4: 11-118480334-G-GTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118480335_118480336insTTTT , CM000673.2:g.118480335_118480336insTTTT	GRCh38
NC_000011.9:g.118351050_118351051insTTTT , CM000673.1:g.118351050_118351051insTTTT	GRCh37
NC_000011.8:g.117856260_117856261insTTTT	NCBI36
NG_027813.1:g.48846_48847insTTTT , LRG_613:g.48846_48847insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.3733+97_3733+98insTTTT	ENSP00000432391.3:n.3733+97_3733+98insTTTT
ENST00000710560.1:c.3733+97_3733+98insTTTT	ENSP00000518343.1:n.3733+97_3733+98insTTTT
ENST00000527869.7:c.1216+97_1216+98insTTTT	ENSP00000432652.3:n.1216+97_1216+98insTTTT
ENST00000533790.3:c.1117+97_1117+98insTTTT	ENSP00000436700.3:n.1117+97_1117+98insTTTT
ENST00000649690.2:c.1441+97_1441+98insTTTT	ENSP00000497372.2:n.1441+97_1441+98insTTTT
ENST00000685719.1:c.615+97_615+98insTTTT
ENST00000691053.1:c.3634+97_3634+98insTTTT	ENSP00000509168.1:n.3634+97_3634+98insTTTT
ENST00000389506.10:c.3634+97_3634+98insTTTT	ENSP00000374157.5:n.3634+97_3634+98insTTTT
ENST00000533790.2:c.886+97_886+98insTTTT	ENSP00000436700.2:n.886+97_886+98insTTTT
ENST00000534358.8:c.3634+97_3634+98insTTTT MANE Select	ENSP00000436786.2:n.3634+97_3634+98insTTTT
ENST00000648261.1:c.2404+97_2404+98insTTTT	ENSP00000498126.1:n.2404+97_2404+98insTTTT
ENST00000649699.1:c.3634+97_3634+98insTTTT	ENSP00000496927.1:n.3634+97_3634+98insTTTT
ENST00000389506.9:c.3634+97_3634+98insTTTT	ENSP00000374157.5:n.3634+97_3634+98insTTTT
ENST00000531904.6:c.3733+97_3733+98insTTTT	ENSP00000432391.2:n.3733+97_3733+98insTTTT
ENST00000534358.5:c.3634+97_3634+98insTTTT	ENSP00000436786.1:n.3634+97_3634+98insTTTT
NM_001197104.1:c.3634+97_3634+98insTTTT , LRG_613t1:c.3634+97_3634+98insTTTT	NP_001184033.1:n.3634+97_3634+98insTTTT
NM_005933.3:c.3634+97_3634+98insTTTT	NP_005924.2:n.3634+97_3634+98insTTTT
XM_006718839.2:c.1117+97_1117+98insTTTT	XP_006718902.2:n.1117+97_1117+98insTTTT
XM_011542829.1:c.3733+97_3733+98insTTTT	XP_011541131.1:n.3733+97_3733+98insTTTT
XM_011542830.1:c.3733+97_3733+98insTTTT	XP_011541132.1:n.3733+97_3733+98insTTTT
XM_011542831.1:c.3733+97_3733+98insTTTT	XP_011541133.1:n.3733+97_3733+98insTTTT
XM_011542832.1:c.1540+97_1540+98insTTTT	XP_011541134.1:n.1540+97_1540+98insTTTT
XM_011542833.1:c.1216+97_1216+98insTTTT	XP_011541135.1:n.1216+97_1216+98insTTTT
XM_006718839.3:c.1117+97_1117+98insTTTT	XP_006718902.2:n.1117+97_1117+98insTTTT
XM_011542829.2:c.3733+97_3733+98insTTTT	XP_011541131.1:n.3733+97_3733+98insTTTT
XM_011542830.2:c.3733+97_3733+98insTTTT	XP_011541132.1:n.3733+97_3733+98insTTTT
XM_011542831.2:c.3733+97_3733+98insTTTT	XP_011541133.1:n.3733+97_3733+98insTTTT
XM_011542833.2:c.1216+97_1216+98insTTTT	XP_011541135.1:n.1216+97_1216+98insTTTT
NM_001197104.2:c.3634+97_3634+98insTTTT MANE Select	NP_001184033.1:n.3634+97_3634+98insTTTT
NM_005933.4:c.3634+97_3634+98insTTTT	NP_005924.2:n.3634+97_3634+98insTTTT