Canonical Allele Identifier: CA382805079

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373922A>C (hg19) ; chr11:g.118503207A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503207A>C , CM000673.2:g.118503207A>C	GRCh38
NC_000011.9:g.118373922A>C , CM000673.1:g.118373922A>C	GRCh37
NC_000011.8:g.117879132A>C	NCBI36
NG_027813.1:g.71718A>C , LRG_613:g.71718A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7414A>C	ENSP00000432391.3:p.Thr2472Pro
ENST00000710560.1:c.7405A>C	ENSP00000518343.1:p.Thr2469Pro
ENST00000649878.2:c.1354A>C	ENSP00000497891.2:p.Thr452Pro
ENST00000685397.1:c.1354A>C	ENSP00000509586.1:p.Thr452Pro
ENST00000686370.1:c.1354A>C	ENSP00000509179.1:p.Thr452Pro
ENST00000689424.1:c.1612A>C	ENSP00000509852.1:p.Thr538Pro
ENST00000691053.1:c.7387A>C	ENSP00000509168.1:p.Thr2463Pro
ENST00000389506.10:c.7306A>C	ENSP00000374157.5:p.Thr2436Pro
ENST00000528278.2:n.6657A>C
ENST00000534358.8:c.7315A>C MANE Select	ENSP00000436786.2:p.Thr2439Pro
ENST00000649699.1:c.7192A>C	ENSP00000496927.1:p.Thr2398Pro
ENST00000389506.9:c.7306A>C	ENSP00000374157.5:p.Thr2436Pro
ENST00000528278.1:n.1442A>C
ENST00000534358.5:c.7315A>C	ENSP00000436786.1:p.Thr2439Pro
NM_001197104.1:c.7315A>C , LRG_613t1:c.7315A>C	NP_001184033.1:p.Thr2439Pro
NM_005933.3:c.7306A>C	NP_005924.2:p.Thr2436Pro
XM_006718839.2:c.4798A>C	XP_006718902.2:p.Thr1600Pro
XM_011542829.1:c.7414A>C	XP_011541131.1:p.Thr2472Pro
XM_011542830.1:c.7411A>C	XP_011541132.1:p.Thr2471Pro
XM_011542831.1:c.7405A>C	XP_011541133.1:p.Thr2469Pro
XM_011542832.1:c.5221A>C	XP_011541134.1:p.Thr1741Pro
XM_011542833.1:c.4897A>C	XP_011541135.1:p.Thr1633Pro
XM_006718839.3:c.4798A>C	XP_006718902.2:p.Thr1600Pro
XM_011542829.2:c.7414A>C	XP_011541131.1:p.Thr2472Pro
XM_011542830.2:c.7411A>C	XP_011541132.1:p.Thr2471Pro
XM_011542831.2:c.7405A>C	XP_011541133.1:p.Thr2469Pro
XM_011542833.2:c.4897A>C	XP_011541135.1:p.Thr1633Pro
NM_001197104.2:c.7315A>C MANE Select	NP_001184033.1:p.Thr2439Pro
NM_005933.4:c.7306A>C	NP_005924.2:p.Thr2436Pro