Canonical Allele Identifier: CA382806028

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374172C>A (hg19) ; chr11:g.118503457C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503457C>A , CM000673.2:g.118503457C>A	GRCh38
NC_000011.9:g.118374172C>A , CM000673.1:g.118374172C>A	GRCh37
NC_000011.8:g.117879382C>A	NCBI36
NG_027813.1:g.71968C>A , LRG_613:g.71968C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.7664C>A	ENSP00000432391.3:p.Thr2555Lys
ENST00000710560.1:c.7655C>A	ENSP00000518343.1:p.Thr2552Lys
ENST00000649878.2:c.1604C>A	ENSP00000497891.2:p.Thr535Lys
ENST00000685397.1:c.1604C>A	ENSP00000509586.1:p.Thr535Lys
ENST00000686370.1:c.1604C>A	ENSP00000509179.1:p.Thr535Lys
ENST00000689424.1:c.1862C>A	ENSP00000509852.1:p.Thr621Lys
ENST00000691053.1:c.7637C>A	ENSP00000509168.1:p.Thr2546Lys
ENST00000389506.10:c.7556C>A	ENSP00000374157.5:p.Thr2519Lys
ENST00000528278.2:n.6907C>A
ENST00000534358.8:c.7565C>A MANE Select	ENSP00000436786.2:p.Thr2522Lys
ENST00000649699.1:c.7442C>A	ENSP00000496927.1:p.Thr2481Lys
ENST00000389506.9:c.7556C>A	ENSP00000374157.5:p.Thr2519Lys
ENST00000528278.1:n.1692C>A
ENST00000534358.5:c.7565C>A	ENSP00000436786.1:p.Thr2522Lys
NM_001197104.1:c.7565C>A , LRG_613t1:c.7565C>A	NP_001184033.1:p.Thr2522Lys
NM_005933.3:c.7556C>A	NP_005924.2:p.Thr2519Lys
XM_006718839.2:c.5048C>A	XP_006718902.2:p.Thr1683Lys
XM_011542829.1:c.7664C>A	XP_011541131.1:p.Thr2555Lys
XM_011542830.1:c.7661C>A	XP_011541132.1:p.Thr2554Lys
XM_011542831.1:c.7655C>A	XP_011541133.1:p.Thr2552Lys
XM_011542832.1:c.5471C>A	XP_011541134.1:p.Thr1824Lys
XM_011542833.1:c.5147C>A	XP_011541135.1:p.Thr1716Lys
XM_006718839.3:c.5048C>A	XP_006718902.2:p.Thr1683Lys
XM_011542829.2:c.7664C>A	XP_011541131.1:p.Thr2555Lys
XM_011542830.2:c.7661C>A	XP_011541132.1:p.Thr2554Lys
XM_011542831.2:c.7655C>A	XP_011541133.1:p.Thr2552Lys
XM_011542833.2:c.5147C>A	XP_011541135.1:p.Thr1716Lys
NM_001197104.2:c.7565C>A MANE Select	NP_001184033.1:p.Thr2522Lys
NM_005933.4:c.7556C>A	NP_005924.2:p.Thr2519Lys