Canonical Allele Identifier: CA477359721

Gene: KMT2A

Linked Data

• dbSNP Id: rs2134392941
• MyVariant Identifiers: chr11:g.118374176C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503461C>G , CM000673.2:g.118503461C>G	GRCh38
NC_000011.9:g.118374176C>G , CM000673.1:g.118374176C>G	GRCh37
NC_000011.8:g.117879386C>G	NCBI36
NG_027813.1:g.71972C>G , LRG_613:g.71972C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.7668C>G	ENSP00000432391.3:p.Val2556=
ENST00000710560.1:c.7659C>G	ENSP00000518343.1:p.Val2553=
ENST00000649878.2:c.1608C>G	ENSP00000497891.2:p.Val536=
ENST00000685397.1:c.1608C>G	ENSP00000509586.1:p.Val536=
ENST00000686370.1:c.1608C>G	ENSP00000509179.1:p.Val536=
ENST00000689424.1:c.1866C>G	ENSP00000509852.1:p.Val622=
ENST00000691053.1:c.7641C>G	ENSP00000509168.1:p.Val2547=
ENST00000389506.10:c.7560C>G	ENSP00000374157.5:p.Val2520=
ENST00000528278.2:n.6911C>G
ENST00000534358.8:c.7569C>G MANE Select	ENSP00000436786.2:p.Val2523=
ENST00000649699.1:c.7446C>G	ENSP00000496927.1:p.Val2482=
ENST00000389506.9:c.7560C>G	ENSP00000374157.5:p.Val2520=
ENST00000528278.1:n.1696C>G
ENST00000534358.5:c.7569C>G	ENSP00000436786.1:p.Val2523=
NM_001197104.1:c.7569C>G , LRG_613t1:c.7569C>G	NP_001184033.1:p.Val2523=
NM_005933.3:c.7560C>G	NP_005924.2:p.Val2520=
XM_006718839.2:c.5052C>G	XP_006718902.2:p.Val1684=
XM_011542829.1:c.7668C>G	XP_011541131.1:p.Val2556=
XM_011542830.1:c.7665C>G	XP_011541132.1:p.Val2555=
XM_011542831.1:c.7659C>G	XP_011541133.1:p.Val2553=
XM_011542832.1:c.5475C>G	XP_011541134.1:p.Val1825=
XM_011542833.1:c.5151C>G	XP_011541135.1:p.Val1717=
XM_006718839.3:c.5052C>G	XP_006718902.2:p.Val1684=
XM_011542829.2:c.7668C>G	XP_011541131.1:p.Val2556=
XM_011542830.2:c.7665C>G	XP_011541132.1:p.Val2555=
XM_011542831.2:c.7659C>G	XP_011541133.1:p.Val2553=
XM_011542833.2:c.5151C>G	XP_011541135.1:p.Val1717=
NM_001197104.2:c.7569C>G MANE Select	NP_001184033.1:p.Val2523=
NM_005933.4:c.7560C>G	NP_005924.2:p.Val2520=