Canonical Allele Identifier: CA602140281

Gene: KMT2A

Linked Data

• dbSNP Id: rs1188619979
• gnomAD v2: 11-118351162-TTTAAATTTATA-T
• gnomAD v3: 11-118480447-TTTAAATTTATA-T
• gnomAD v4: 11-118480447-TTTAAATTTATA-T
• MyVariant Identifiers: chr11:g.118351163_118351173del (hg19) ; chr11:g.118480448_118480458del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118480449_118480459del , CM000673.2:g.118480449_118480459del	GRCh38
NC_000011.9:g.118351164_118351174del , CM000673.1:g.118351164_118351174del	GRCh37
NC_000011.8:g.117856374_117856384del	NCBI36
NG_027813.1:g.48960_48970del , LRG_613:g.48960_48970del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.3733+211_3733+221del	ENSP00000432391.3:n.3733+211_3733+221del
ENST00000710560.1:c.3733+211_3733+221del	ENSP00000518343.1:n.3733+211_3733+221del
ENST00000527869.7:c.1216+211_1216+221del	ENSP00000432652.3:n.1216+211_1216+221del
ENST00000533790.3:c.1117+211_1117+221del	ENSP00000436700.3:n.1117+211_1117+221del
ENST00000649690.2:c.1441+211_1441+221del	ENSP00000497372.2:n.1441+211_1441+221del
ENST00000685719.1:c.615+211_615+221del
ENST00000691053.1:c.3634+211_3634+221del	ENSP00000509168.1:n.3634+211_3634+221del
ENST00000389506.10:c.3634+211_3634+221del	ENSP00000374157.5:n.3634+211_3634+221del
ENST00000533790.2:c.886+211_886+221del	ENSP00000436700.2:n.886+211_886+221del
ENST00000534358.8:c.3634+211_3634+221del MANE Select	ENSP00000436786.2:n.3634+211_3634+221del
ENST00000648261.1:c.2404+211_2404+221del	ENSP00000498126.1:n.2404+211_2404+221del
ENST00000649699.1:c.3634+211_3634+221del	ENSP00000496927.1:n.3634+211_3634+221del
ENST00000389506.9:c.3634+211_3634+221del	ENSP00000374157.5:n.3634+211_3634+221del
ENST00000531904.6:c.3733+211_3733+221del	ENSP00000432391.2:n.3733+211_3733+221del
ENST00000534358.5:c.3634+211_3634+221del	ENSP00000436786.1:n.3634+211_3634+221del
NM_001197104.1:c.3634+211_3634+221del , LRG_613t1:c.3634+211_3634+221del	NP_001184033.1:n.3634+211_3634+221del
NM_005933.3:c.3634+211_3634+221del	NP_005924.2:n.3634+211_3634+221del
XM_006718839.2:c.1117+211_1117+221del	XP_006718902.2:n.1117+211_1117+221del
XM_011542829.1:c.3733+211_3733+221del	XP_011541131.1:n.3733+211_3733+221del
XM_011542830.1:c.3733+211_3733+221del	XP_011541132.1:n.3733+211_3733+221del
XM_011542831.1:c.3733+211_3733+221del	XP_011541133.1:n.3733+211_3733+221del
XM_011542832.1:c.1540+211_1540+221del	XP_011541134.1:n.1540+211_1540+221del
XM_011542833.1:c.1216+211_1216+221del	XP_011541135.1:n.1216+211_1216+221del
XM_006718839.3:c.1117+211_1117+221del	XP_006718902.2:n.1117+211_1117+221del
XM_011542829.2:c.3733+211_3733+221del	XP_011541131.1:n.3733+211_3733+221del
XM_011542830.2:c.3733+211_3733+221del	XP_011541132.1:n.3733+211_3733+221del
XM_011542831.2:c.3733+211_3733+221del	XP_011541133.1:n.3733+211_3733+221del
XM_011542833.2:c.1216+211_1216+221del	XP_011541135.1:n.1216+211_1216+221del
NM_001197104.2:c.3634+211_3634+221del MANE Select	NP_001184033.1:n.3634+211_3634+221del
NM_005933.4:c.3634+211_3634+221del	NP_005924.2:n.3634+211_3634+221del