Canonical Allele Identifier: CA382833675

Gene: KMT2A TTC36-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118520021C>A , CM000673.2:g.118520021C>A	GRCh38
NC_000011.9:g.118390736C>A , CM000673.1:g.118390736C>A	GRCh37
NC_000011.8:g.117895946C>A	NCBI36
NG_027813.1:g.88532C>A , LRG_613:g.88532C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000531904.7:c.11485C>A (KMT2A)	ENSP00000432391.3:p.Pro3829Thr
ENST00000710560.1:c.11476C>A (KMT2A)	ENSP00000518343.1:p.Pro3826Thr
ENST00000686588.1:c.482C>A (KMT2A)
ENST00000691053.1:c.11458C>A (KMT2A)	ENSP00000509168.1:p.Pro3820Thr
ENST00000389506.10:c.11377C>A (KMT2A)	ENSP00000374157.5:p.Pro3793Thr
ENST00000525408.2:n.301C>A (KMT2A)
ENST00000527839.2:n.886C>A (KMT2A)
ENST00000534358.8:c.11386C>A (KMT2A) MANE Select	ENSP00000436786.2:p.Pro3796Thr
ENST00000648565.1:n.622C>A (KMT2A)
ENST00000649699.1:c.11263C>A (KMT2A)	ENSP00000496927.1:p.Pro3755Thr
ENST00000389506.9:c.11377C>A (KMT2A)	ENSP00000374157.5:p.Pro3793Thr
ENST00000525408.1:n.299C>A (KMT2A)
ENST00000527839.1:n.187C>A (KMT2A)
ENST00000534358.5:c.11386C>A (KMT2A)	ENSP00000436786.1:p.Pro3796Thr
NM_001197104.1:c.11386C>A , LRG_613t1:c.11386C>A (KMT2A)	NP_001184033.1:p.Pro3796Thr
NM_005933.3:c.11377C>A (KMT2A)	NP_005924.2:p.Pro3793Thr
NR_120572.1:n.429-325G>T (TTC36-AS1)
NR_120573.1:n.322-325G>T (TTC36-AS1)
NR_120574.1:n.321+1245G>T (TTC36-AS1)
NR_120575.1:n.342-325G>T (TTC36-AS1)
NR_120576.1:n.154-325G>T (TTC36-AS1)
XM_006718839.2:c.8869C>A (KMT2A)	XP_006718902.2:p.Pro2957Thr
XM_011542829.1:c.11485C>A (KMT2A)	XP_011541131.1:p.Pro3829Thr
XM_011542830.1:c.11482C>A (KMT2A)	XP_011541132.1:p.Pro3828Thr
XM_011542831.1:c.11476C>A (KMT2A)	XP_011541133.1:p.Pro3826Thr
XM_011542832.1:c.9292C>A (KMT2A)	XP_011541134.1:p.Pro3098Thr
XM_011542833.1:c.8968C>A (KMT2A)	XP_011541135.1:p.Pro2990Thr
XM_006718839.3:c.8869C>A (KMT2A)	XP_006718902.2:p.Pro2957Thr
XM_011542829.2:c.11485C>A (KMT2A)	XP_011541131.1:p.Pro3829Thr
XM_011542830.2:c.11482C>A (KMT2A)	XP_011541132.1:p.Pro3828Thr
XM_011542831.2:c.11476C>A (KMT2A)	XP_011541133.1:p.Pro3826Thr
XM_011542833.2:c.8968C>A (KMT2A)	XP_011541135.1:p.Pro2990Thr
NM_001197104.2:c.11386C>A (KMT2A) MANE Select	NP_001184033.1:p.Pro3796Thr
NM_005933.4:c.11377C>A (KMT2A)	NP_005924.2:p.Pro3793Thr