Canonical Allele Identifier: CA6304952
Gene: KMT2A HGNC NCBI
TTC36-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.118520026T>C , CM000673.2:g.118520026T>C GRCh38
NC_000011.9:g.118390741T>C , CM000673.1:g.118390741T>C GRCh37
NC_000011.8:g.117895951T>C NCBI36
NG_027813.1:g.88537T>C , LRG_613:g.88537T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001197104.2:c.11391T>C (KMT2A) MANE Select NP_001184033.1:p.Asn3797=
ENST00000534358.8:c.11391T>C (KMT2A) MANE Select ENSP00000436786.2:p.Asn3797=
NM_001197104.1:c.11391T>C , LRG_613t1:c.11391T>C (KMT2A) NP_001184033.1:p.Asn3797=
NM_005933.3:c.11382T>C (KMT2A) NP_005924.2:p.Asn3794=
NM_005933.4:c.11382T>C (KMT2A) NP_005924.2:p.Asn3794=
NR_120572.1:n.429-330A>G (TTC36-AS1)
NR_120573.1:n.322-330A>G (TTC36-AS1)
NR_120574.1:n.321+1240A>G (TTC36-AS1)
NR_120575.1:n.342-330A>G (TTC36-AS1)
NR_120576.1:n.154-330A>G (TTC36-AS1)
ENST00000389506.10:c.11382T>C (KMT2A) ENSP00000374157.5:p.Asn3794=
ENST00000389506.9:c.11382T>C (KMT2A) ENSP00000374157.5:p.Asn3794=
ENST00000525408.1:n.304T>C (KMT2A)
ENST00000525408.2:n.306T>C (KMT2A)
ENST00000527839.1:n.192T>C (KMT2A)
ENST00000527839.2:n.891T>C (KMT2A)
ENST00000531904.7:c.11490T>C (KMT2A) ENSP00000432391.3:p.Asn3830=
ENST00000534358.5:c.11391T>C (KMT2A) ENSP00000436786.1:p.Asn3797=
ENST00000648565.1:n.627T>C (KMT2A)
ENST00000649699.1:c.11268T>C (KMT2A) ENSP00000496927.1:p.Asn3756=
ENST00000686588.1:c.487T>C (KMT2A)
ENST00000691053.1:c.11463T>C (KMT2A) ENSP00000509168.1:p.Asn3821=
ENST00000710560.1:c.11481T>C (KMT2A) ENSP00000518343.1:p.Asn3827=
XM_006718839.2:c.8874T>C (KMT2A) XP_006718902.2:p.Asn2958=
XM_006718839.3:c.8874T>C (KMT2A) XP_006718902.2:p.Asn2958=
XM_011542829.1:c.11490T>C (KMT2A) XP_011541131.1:p.Asn3830=
XM_011542829.2:c.11490T>C (KMT2A) XP_011541131.1:p.Asn3830=
XM_011542830.1:c.11487T>C (KMT2A) XP_011541132.1:p.Asn3829=
XM_011542830.2:c.11487T>C (KMT2A) XP_011541132.1:p.Asn3829=
XM_011542831.1:c.11481T>C (KMT2A) XP_011541133.1:p.Asn3827=
XM_011542831.2:c.11481T>C (KMT2A) XP_011541133.1:p.Asn3827=
XM_011542832.1:c.9297T>C (KMT2A) XP_011541134.1:p.Asn3099=
XM_011542833.1:c.8973T>C (KMT2A) XP_011541135.1:p.Asn2991=
XM_011542833.2:c.8973T>C (KMT2A) XP_011541135.1:p.Asn2991=