Canonical Allele Identifier: CA382834263

Gene: KMT2A

Linked Data

• MyVariant Identifiers: chr11:g.118361922C>T (hg19) ; chr11:g.118491207C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118491207C>T , CM000673.2:g.118491207C>T	GRCh38
NC_000011.9:g.118361922C>T , CM000673.1:g.118361922C>T	GRCh37
NC_000011.8:g.117867132C>T	NCBI36
NG_027813.1:g.59718C>T , LRG_613:g.59718C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.4807C>T	ENSP00000432391.3:p.Pro1603Ser
ENST00000710560.1:c.4807C>T	ENSP00000518343.1:p.Pro1603Ser
ENST00000685498.1:c.484C>T	ENSP00000509293.1:p.Pro162Ser
ENST00000691053.1:c.4708C>T	ENSP00000509168.1:p.Pro1570Ser
ENST00000389506.10:c.4708C>T	ENSP00000374157.5:p.Pro1570Ser
ENST00000534358.8:c.4708C>T MANE Select	ENSP00000436786.2:p.Pro1570Ser
ENST00000649699.1:c.4594C>T	ENSP00000496927.1:p.Pro1532Ser
ENST00000389506.9:c.4708C>T	ENSP00000374157.5:p.Pro1570Ser
ENST00000392873.3:c.844C>T	ENSP00000376612.3:p.Pro282Ser
ENST00000534358.5:c.4708C>T	ENSP00000436786.1:p.Pro1570Ser
NM_001197104.1:c.4708C>T , LRG_613t1:c.4708C>T	NP_001184033.1:p.Pro1570Ser
NM_005933.3:c.4708C>T	NP_005924.2:p.Pro1570Ser
XM_006718839.2:c.2191C>T	XP_006718902.2:p.Pro731Ser
XM_011542829.1:c.4807C>T	XP_011541131.1:p.Pro1603Ser
XM_011542830.1:c.4804C>T	XP_011541132.1:p.Pro1602Ser
XM_011542831.1:c.4807C>T	XP_011541133.1:p.Pro1603Ser
XM_011542832.1:c.2614C>T	XP_011541134.1:p.Pro872Ser
XM_011542833.1:c.2290C>T	XP_011541135.1:p.Pro764Ser
XM_006718839.3:c.2191C>T	XP_006718902.2:p.Pro731Ser
XM_011542829.2:c.4807C>T	XP_011541131.1:p.Pro1603Ser
XM_011542830.2:c.4804C>T	XP_011541132.1:p.Pro1602Ser
XM_011542831.2:c.4807C>T	XP_011541133.1:p.Pro1603Ser
XM_011542833.2:c.2290C>T	XP_011541135.1:p.Pro764Ser
NM_001197104.2:c.4708C>T MANE Select	NP_001184033.1:p.Pro1570Ser
NM_005933.4:c.4708C>T	NP_005924.2:p.Pro1570Ser