Canonical Allele Identifier: CA382805530

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374033T>G (hg19) ; chr11:g.118503318T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503318T>G , CM000673.2:g.118503318T>G	GRCh38
NC_000011.9:g.118374033T>G , CM000673.1:g.118374033T>G	GRCh37
NC_000011.8:g.117879243T>G	NCBI36
NG_027813.1:g.71829T>G , LRG_613:g.71829T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7525T>G	ENSP00000432391.3:p.Tyr2509Asp
ENST00000710560.1:c.7516T>G	ENSP00000518343.1:p.Tyr2506Asp
ENST00000649878.2:c.1465T>G	ENSP00000497891.2:p.Tyr489Asp
ENST00000685397.1:c.1465T>G	ENSP00000509586.1:p.Tyr489Asp
ENST00000686370.1:c.1465T>G	ENSP00000509179.1:p.Tyr489Asp
ENST00000689424.1:c.1723T>G	ENSP00000509852.1:p.Tyr575Asp
ENST00000691053.1:c.7498T>G	ENSP00000509168.1:p.Tyr2500Asp
ENST00000389506.10:c.7417T>G	ENSP00000374157.5:p.Tyr2473Asp
ENST00000528278.2:n.6768T>G
ENST00000534358.8:c.7426T>G MANE Select	ENSP00000436786.2:p.Tyr2476Asp
ENST00000649699.1:c.7303T>G	ENSP00000496927.1:p.Tyr2435Asp
ENST00000389506.9:c.7417T>G	ENSP00000374157.5:p.Tyr2473Asp
ENST00000528278.1:n.1553T>G
ENST00000534358.5:c.7426T>G	ENSP00000436786.1:p.Tyr2476Asp
NM_001197104.1:c.7426T>G , LRG_613t1:c.7426T>G	NP_001184033.1:p.Tyr2476Asp
NM_005933.3:c.7417T>G	NP_005924.2:p.Tyr2473Asp
XM_006718839.2:c.4909T>G	XP_006718902.2:p.Tyr1637Asp
XM_011542829.1:c.7525T>G	XP_011541131.1:p.Tyr2509Asp
XM_011542830.1:c.7522T>G	XP_011541132.1:p.Tyr2508Asp
XM_011542831.1:c.7516T>G	XP_011541133.1:p.Tyr2506Asp
XM_011542832.1:c.5332T>G	XP_011541134.1:p.Tyr1778Asp
XM_011542833.1:c.5008T>G	XP_011541135.1:p.Tyr1670Asp
XM_006718839.3:c.4909T>G	XP_006718902.2:p.Tyr1637Asp
XM_011542829.2:c.7525T>G	XP_011541131.1:p.Tyr2509Asp
XM_011542830.2:c.7522T>G	XP_011541132.1:p.Tyr2508Asp
XM_011542831.2:c.7516T>G	XP_011541133.1:p.Tyr2506Asp
XM_011542833.2:c.5008T>G	XP_011541135.1:p.Tyr1670Asp
NM_001197104.2:c.7426T>G MANE Select	NP_001184033.1:p.Tyr2476Asp
NM_005933.4:c.7417T>G	NP_005924.2:p.Tyr2473Asp