Canonical Allele Identifier: CA477359357

Gene: KMT2A

Linked Data

• gnomAD v4: 11-118503257-G-A
• MyVariant Identifiers: chr11:g.118373972G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503257G>A , CM000673.2:g.118503257G>A	GRCh38
NC_000011.9:g.118373972G>A , CM000673.1:g.118373972G>A	GRCh37
NC_000011.8:g.117879182G>A	NCBI36
NG_027813.1:g.71768G>A , LRG_613:g.71768G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7464G>A	ENSP00000432391.3:p.Val2488=
ENST00000710560.1:c.7455G>A	ENSP00000518343.1:p.Val2485=
ENST00000649878.2:c.1404G>A	ENSP00000497891.2:p.Val468=
ENST00000685397.1:c.1404G>A	ENSP00000509586.1:p.Val468=
ENST00000686370.1:c.1404G>A	ENSP00000509179.1:p.Val468=
ENST00000689424.1:c.1662G>A	ENSP00000509852.1:p.Val554=
ENST00000691053.1:c.7437G>A	ENSP00000509168.1:p.Val2479=
ENST00000389506.10:c.7356G>A	ENSP00000374157.5:p.Val2452=
ENST00000528278.2:n.6707G>A
ENST00000534358.8:c.7365G>A MANE Select	ENSP00000436786.2:p.Val2455=
ENST00000649699.1:c.7242G>A	ENSP00000496927.1:p.Val2414=
ENST00000389506.9:c.7356G>A	ENSP00000374157.5:p.Val2452=
ENST00000528278.1:n.1492G>A
ENST00000534358.5:c.7365G>A	ENSP00000436786.1:p.Val2455=
NM_001197104.1:c.7365G>A , LRG_613t1:c.7365G>A	NP_001184033.1:p.Val2455=
NM_005933.3:c.7356G>A	NP_005924.2:p.Val2452=
XM_006718839.2:c.4848G>A	XP_006718902.2:p.Val1616=
XM_011542829.1:c.7464G>A	XP_011541131.1:p.Val2488=
XM_011542830.1:c.7461G>A	XP_011541132.1:p.Val2487=
XM_011542831.1:c.7455G>A	XP_011541133.1:p.Val2485=
XM_011542832.1:c.5271G>A	XP_011541134.1:p.Val1757=
XM_011542833.1:c.4947G>A	XP_011541135.1:p.Val1649=
XM_006718839.3:c.4848G>A	XP_006718902.2:p.Val1616=
XM_011542829.2:c.7464G>A	XP_011541131.1:p.Val2488=
XM_011542830.2:c.7461G>A	XP_011541132.1:p.Val2487=
XM_011542831.2:c.7455G>A	XP_011541133.1:p.Val2485=
XM_011542833.2:c.4947G>A	XP_011541135.1:p.Val1649=
NM_001197104.2:c.7365G>A MANE Select	NP_001184033.1:p.Val2455=
NM_005933.4:c.7356G>A	NP_005924.2:p.Val2452=