Canonical Allele Identifier: CA382806431

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374276T>A (hg19) ; chr11:g.118503561T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503561T>A , CM000673.2:g.118503561T>A	GRCh38
NC_000011.9:g.118374276T>A , CM000673.1:g.118374276T>A	GRCh37
NC_000011.8:g.117879486T>A	NCBI36
NG_027813.1:g.72072T>A , LRG_613:g.72072T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.7768T>A	ENSP00000432391.3:p.Ser2590Thr
ENST00000710560.1:c.7759T>A	ENSP00000518343.1:p.Ser2587Thr
ENST00000649878.2:c.1708T>A	ENSP00000497891.2:p.Ser570Thr
ENST00000685397.1:c.1708T>A	ENSP00000509586.1:p.Ser570Thr
ENST00000686370.1:c.1708T>A	ENSP00000509179.1:p.Ser570Thr
ENST00000689424.1:c.1966T>A	ENSP00000509852.1:p.Ser656Thr
ENST00000691053.1:c.7741T>A	ENSP00000509168.1:p.Ser2581Thr
ENST00000389506.10:c.7660T>A	ENSP00000374157.5:p.Ser2554Thr
ENST00000528278.2:n.7011T>A
ENST00000534358.8:c.7669T>A MANE Select	ENSP00000436786.2:p.Ser2557Thr
ENST00000649699.1:c.7546T>A	ENSP00000496927.1:p.Ser2516Thr
ENST00000389506.9:c.7660T>A	ENSP00000374157.5:p.Ser2554Thr
ENST00000528278.1:n.1796T>A
ENST00000534358.5:c.7669T>A	ENSP00000436786.1:p.Ser2557Thr
NM_001197104.1:c.7669T>A , LRG_613t1:c.7669T>A	NP_001184033.1:p.Ser2557Thr
NM_005933.3:c.7660T>A	NP_005924.2:p.Ser2554Thr
XM_006718839.2:c.5152T>A	XP_006718902.2:p.Ser1718Thr
XM_011542829.1:c.7768T>A	XP_011541131.1:p.Ser2590Thr
XM_011542830.1:c.7765T>A	XP_011541132.1:p.Ser2589Thr
XM_011542831.1:c.7759T>A	XP_011541133.1:p.Ser2587Thr
XM_011542832.1:c.5575T>A	XP_011541134.1:p.Ser1859Thr
XM_011542833.1:c.5251T>A	XP_011541135.1:p.Ser1751Thr
XM_006718839.3:c.5152T>A	XP_006718902.2:p.Ser1718Thr
XM_011542829.2:c.7768T>A	XP_011541131.1:p.Ser2590Thr
XM_011542830.2:c.7765T>A	XP_011541132.1:p.Ser2589Thr
XM_011542831.2:c.7759T>A	XP_011541133.1:p.Ser2587Thr
XM_011542833.2:c.5251T>A	XP_011541135.1:p.Ser1751Thr
NM_001197104.2:c.7669T>A MANE Select	NP_001184033.1:p.Ser2557Thr
NM_005933.4:c.7660T>A	NP_005924.2:p.Ser2554Thr