Canonical Allele Identifier: CA382805083

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118373923C>A (hg19) ; chr11:g.118503208C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118503208C>A , CM000673.2:g.118503208C>A	GRCh38
NC_000011.9:g.118373923C>A , CM000673.1:g.118373923C>A	GRCh37
NC_000011.8:g.117879133C>A	NCBI36
NG_027813.1:g.71719C>A , LRG_613:g.71719C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.7415C>A	ENSP00000432391.3:p.Thr2472Asn
ENST00000710560.1:c.7406C>A	ENSP00000518343.1:p.Thr2469Asn
ENST00000649878.2:c.1355C>A	ENSP00000497891.2:p.Thr452Asn
ENST00000685397.1:c.1355C>A	ENSP00000509586.1:p.Thr452Asn
ENST00000686370.1:c.1355C>A	ENSP00000509179.1:p.Thr452Asn
ENST00000689424.1:c.1613C>A	ENSP00000509852.1:p.Thr538Asn
ENST00000691053.1:c.7388C>A	ENSP00000509168.1:p.Thr2463Asn
ENST00000389506.10:c.7307C>A	ENSP00000374157.5:p.Thr2436Asn
ENST00000528278.2:n.6658C>A
ENST00000534358.8:c.7316C>A MANE Select	ENSP00000436786.2:p.Thr2439Asn
ENST00000649699.1:c.7193C>A	ENSP00000496927.1:p.Thr2398Asn
ENST00000389506.9:c.7307C>A	ENSP00000374157.5:p.Thr2436Asn
ENST00000528278.1:n.1443C>A
ENST00000534358.5:c.7316C>A	ENSP00000436786.1:p.Thr2439Asn
NM_001197104.1:c.7316C>A , LRG_613t1:c.7316C>A	NP_001184033.1:p.Thr2439Asn
NM_005933.3:c.7307C>A	NP_005924.2:p.Thr2436Asn
XM_006718839.2:c.4799C>A	XP_006718902.2:p.Thr1600Asn
XM_011542829.1:c.7415C>A	XP_011541131.1:p.Thr2472Asn
XM_011542830.1:c.7412C>A	XP_011541132.1:p.Thr2471Asn
XM_011542831.1:c.7406C>A	XP_011541133.1:p.Thr2469Asn
XM_011542832.1:c.5222C>A	XP_011541134.1:p.Thr1741Asn
XM_011542833.1:c.4898C>A	XP_011541135.1:p.Thr1633Asn
XM_006718839.3:c.4799C>A	XP_006718902.2:p.Thr1600Asn
XM_011542829.2:c.7415C>A	XP_011541131.1:p.Thr2472Asn
XM_011542830.2:c.7412C>A	XP_011541132.1:p.Thr2471Asn
XM_011542831.2:c.7406C>A	XP_011541133.1:p.Thr2469Asn
XM_011542833.2:c.4898C>A	XP_011541135.1:p.Thr1633Asn
NM_001197104.2:c.7316C>A MANE Select	NP_001184033.1:p.Thr2439Asn
NM_005933.4:c.7307C>A	NP_005924.2:p.Thr2436Asn