Canonical Allele Identifier: CA382815873

Gene: KMT2A

Linked Data

• dbSNP Id: rs2134269842
• MyVariant Identifiers: chr11:g.118344395C>T (hg19) ; chr11:g.118473680C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118473680C>T , CM000673.2:g.118473680C>T	GRCh38
NC_000011.9:g.118344395C>T , CM000673.1:g.118344395C>T	GRCh37
NC_000011.8:g.117849605C>T	NCBI36
NG_027813.1:g.42191C>T , LRG_613:g.42191C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.2620C>T	ENSP00000432391.3:p.Pro874Ser
ENST00000710560.1:c.2620C>T	ENSP00000518343.1:p.Pro874Ser
ENST00000527869.7:c.602-499C>T	ENSP00000432652.3:n.602-499C>T
ENST00000533790.3:c.503-499C>T	ENSP00000436700.3:n.503-499C>T
ENST00000649690.2:c.827-499C>T	ENSP00000497372.2:n.827-499C>T
ENST00000691053.1:c.2521C>T	ENSP00000509168.1:p.Pro841Ser
ENST00000389506.10:c.2521C>T	ENSP00000374157.5:p.Pro841Ser
ENST00000533790.2:c.272-499C>T	ENSP00000436700.2:n.272-499C>T
ENST00000534358.8:c.2521C>T MANE Select	ENSP00000436786.2:p.Pro841Ser
ENST00000648261.1:c.1291C>T	ENSP00000498126.1:p.Pro431Ser
ENST00000649690.1:c.413-499C>T	ENSP00000497372.1:n.413-499C>T
ENST00000649699.1:c.2521C>T	ENSP00000496927.1:p.Pro841Ser
ENST00000389506.9:c.2521C>T	ENSP00000374157.5:p.Pro841Ser
ENST00000527869.6:c.353-499C>T	ENSP00000432652.2:n.353-499C>T
ENST00000531904.6:c.2620C>T	ENSP00000432391.2:p.Pro874Ser
ENST00000533790.1:c.254-499C>T	ENSP00000436700.1:n.254-499C>T
ENST00000534358.5:c.2521C>T	ENSP00000436786.1:p.Pro841Ser
NM_001197104.1:c.2521C>T , LRG_613t1:c.2521C>T	NP_001184033.1:p.Pro841Ser
NM_005933.3:c.2521C>T	NP_005924.2:p.Pro841Ser
XM_006718839.2:c.503-499C>T	XP_006718902.2:n.503-499C>T
XM_011542829.1:c.2620C>T	XP_011541131.1:p.Pro874Ser
XM_011542830.1:c.2620C>T	XP_011541132.1:p.Pro874Ser
XM_011542831.1:c.2620C>T	XP_011541133.1:p.Pro874Ser
XM_011542832.1:c.926-499C>T	XP_011541134.1:n.926-499C>T
XM_011542833.1:c.602-499C>T	XP_011541135.1:n.602-499C>T
XM_006718839.3:c.503-499C>T	XP_006718902.2:n.503-499C>T
XM_011542829.2:c.2620C>T	XP_011541131.1:p.Pro874Ser
XM_011542830.2:c.2620C>T	XP_011541132.1:p.Pro874Ser
XM_011542831.2:c.2620C>T	XP_011541133.1:p.Pro874Ser
XM_011542833.2:c.602-499C>T	XP_011541135.1:n.602-499C>T
NM_001197104.2:c.2521C>T MANE Select	NP_001184033.1:p.Pro841Ser
NM_005933.4:c.2521C>T	NP_005924.2:p.Pro841Ser