Canonical Allele Identifier: CA6304904

Gene: KMT2A TTC36-AS1

Linked Data

• dbSNP Id: rs782477344
• ExAC: 11:118382678 C / T
• gnomAD v2: 11-118382678-C-T
• gnomAD v4: 11-118511963-C-T
• MyVariant Identifiers: chr11:g.118382678C>T (hg19) ; chr11:g.118511963C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118511963C>T , CM000673.2:g.118511963C>T	GRCh38
NC_000011.9:g.118382678C>T , CM000673.1:g.118382678C>T	GRCh37
NC_000011.8:g.117887888C>T	NCBI36
NG_027813.1:g.80474C>T , LRG_613:g.80474C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000531904.7:c.11183C>T (KMT2A)	ENSP00000432391.3:p.Ser3728Leu
ENST00000710560.1:c.11174C>T (KMT2A)	ENSP00000518343.1:p.Ser3725Leu
ENST00000649878.2:c.5100C>T (KMT2A)	ENSP00000497891.2:n.5100C>T
ENST00000685397.1:c.5042C>T (KMT2A)	ENSP00000509586.1:p.Ser1681Leu
ENST00000686370.1:c.5144C>T (KMT2A)	ENSP00000509179.1:p.Ser1715Leu
ENST00000686588.1:c.184C>T (KMT2A)
ENST00000691053.1:c.11156C>T (KMT2A)	ENSP00000509168.1:p.Ser3719Leu
ENST00000389506.10:c.11075C>T (KMT2A)	ENSP00000374157.5:p.Ser3692Leu
ENST00000527839.2:n.584C>T (KMT2A)
ENST00000534358.8:c.11084C>T (KMT2A) MANE Select	ENSP00000436786.2:p.Ser3695Leu
ENST00000534678.3:n.542C>T (KMT2A)
ENST00000648565.1:n.320C>T (KMT2A)
ENST00000649699.1:c.10961C>T (KMT2A)	ENSP00000496927.1:p.Ser3654Leu
ENST00000649878.1:c.408C>T (KMT2A)	ENSP00000497891.1:n.408C>T
ENST00000389506.9:c.11075C>T (KMT2A)	ENSP00000374157.5:p.Ser3692Leu
ENST00000534358.5:c.11084C>T (KMT2A)	ENSP00000436786.1:p.Ser3695Leu
ENST00000534678.2:n.186C>T (KMT2A)
NM_001197104.1:c.11084C>T , LRG_613t1:c.11084C>T (KMT2A)	NP_001184033.1:p.Ser3695Leu
NM_005933.3:c.11075C>T (KMT2A)	NP_005924.2:p.Ser3692Leu
NR_120574.1:n.459G>A (TTC36-AS1)
XM_006718839.2:c.8567C>T (KMT2A)	XP_006718902.2:p.Ser2856Leu
XM_011542829.1:c.11183C>T (KMT2A)	XP_011541131.1:p.Ser3728Leu
XM_011542830.1:c.11180C>T (KMT2A)	XP_011541132.1:p.Ser3727Leu
XM_011542831.1:c.11174C>T (KMT2A)	XP_011541133.1:p.Ser3725Leu
XM_011542832.1:c.8990C>T (KMT2A)	XP_011541134.1:p.Ser2997Leu
XM_011542833.1:c.8666C>T (KMT2A)	XP_011541135.1:p.Ser2889Leu
XM_006718839.3:c.8567C>T (KMT2A)	XP_006718902.2:p.Ser2856Leu
XM_011542829.2:c.11183C>T (KMT2A)	XP_011541131.1:p.Ser3728Leu
XM_011542830.2:c.11180C>T (KMT2A)	XP_011541132.1:p.Ser3727Leu
XM_011542831.2:c.11174C>T (KMT2A)	XP_011541133.1:p.Ser3725Leu
XM_011542833.2:c.8666C>T (KMT2A)	XP_011541135.1:p.Ser2889Leu
NM_001197104.2:c.11084C>T (KMT2A) MANE Select	NP_001184033.1:p.Ser3695Leu
NM_005933.4:c.11075C>T (KMT2A)	NP_005924.2:p.Ser3692Leu