Canonical Allele Identifier: CA382805490

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118374024A>C (hg19) ; chr11:g.118503309A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503309A>C , CM000673.2:g.118503309A>C	GRCh38
NC_000011.9:g.118374024A>C , CM000673.1:g.118374024A>C	GRCh37
NC_000011.8:g.117879234A>C	NCBI36
NG_027813.1:g.71820A>C , LRG_613:g.71820A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7516A>C	ENSP00000432391.3:p.Thr2506Pro
ENST00000710560.1:c.7507A>C	ENSP00000518343.1:p.Thr2503Pro
ENST00000649878.2:c.1456A>C	ENSP00000497891.2:p.Thr486Pro
ENST00000685397.1:c.1456A>C	ENSP00000509586.1:p.Thr486Pro
ENST00000686370.1:c.1456A>C	ENSP00000509179.1:p.Thr486Pro
ENST00000689424.1:c.1714A>C	ENSP00000509852.1:p.Thr572Pro
ENST00000691053.1:c.7489A>C	ENSP00000509168.1:p.Thr2497Pro
ENST00000389506.10:c.7408A>C	ENSP00000374157.5:p.Thr2470Pro
ENST00000528278.2:n.6759A>C
ENST00000534358.8:c.7417A>C MANE Select	ENSP00000436786.2:p.Thr2473Pro
ENST00000649699.1:c.7294A>C	ENSP00000496927.1:p.Thr2432Pro
ENST00000389506.9:c.7408A>C	ENSP00000374157.5:p.Thr2470Pro
ENST00000528278.1:n.1544A>C
ENST00000534358.5:c.7417A>C	ENSP00000436786.1:p.Thr2473Pro
NM_001197104.1:c.7417A>C , LRG_613t1:c.7417A>C	NP_001184033.1:p.Thr2473Pro
NM_005933.3:c.7408A>C	NP_005924.2:p.Thr2470Pro
XM_006718839.2:c.4900A>C	XP_006718902.2:p.Thr1634Pro
XM_011542829.1:c.7516A>C	XP_011541131.1:p.Thr2506Pro
XM_011542830.1:c.7513A>C	XP_011541132.1:p.Thr2505Pro
XM_011542831.1:c.7507A>C	XP_011541133.1:p.Thr2503Pro
XM_011542832.1:c.5323A>C	XP_011541134.1:p.Thr1775Pro
XM_011542833.1:c.4999A>C	XP_011541135.1:p.Thr1667Pro
XM_006718839.3:c.4900A>C	XP_006718902.2:p.Thr1634Pro
XM_011542829.2:c.7516A>C	XP_011541131.1:p.Thr2506Pro
XM_011542830.2:c.7513A>C	XP_011541132.1:p.Thr2505Pro
XM_011542831.2:c.7507A>C	XP_011541133.1:p.Thr2503Pro
XM_011542833.2:c.4999A>C	XP_011541135.1:p.Thr1667Pro
NM_001197104.2:c.7417A>C MANE Select	NP_001184033.1:p.Thr2473Pro
NM_005933.4:c.7408A>C	NP_005924.2:p.Thr2470Pro