Canonical Allele Identifier: CA458884948

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845761T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148676T>A , CM000669.2:g.152148676T>A	GRCh38
NC_000007.13:g.151845761T>A , CM000669.1:g.151845761T>A	GRCh37
NC_000007.12:g.151476694T>A	NCBI36
NG_033948.1:g.292330A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682040.1:c.1439A>T
ENST00000682116.1:n.2383A>T
ENST00000682283.1:c.13422A>T	ENSP00000507485.1:p.Ala4474=
ENST00000682629.1:n.2551A>T
ENST00000683120.1:n.8443A>T
ENST00000683178.1:c.3824A>T
ENST00000683200.1:c.10761A>T	ENSP00000508052.1:p.Ala3587=
ENST00000683337.1:n.4881A>T
ENST00000683502.1:c.3896A>T
ENST00000683621.1:n.2017A>T
ENST00000683640.1:n.1967A>T
ENST00000684069.1:c.1668A>T	ENSP00000507650.1:p.Ala556=
ENST00000684261.1:c.8148A>T	ENSP00000508097.1:p.Ala2716=
ENST00000684391.1:n.9A>T
ENST00000684649.1:c.3896A>T
ENST00000262189.11:c.13251A>T MANE Select	ENSP00000262189.6:p.Ala4417=
ENST00000360104.8:c.9038A>T
ENST00000418061.2:c.3893A>T
ENST00000424877.6:c.3827A>T
ENST00000679393.1:n.7962A>T
ENST00000679560.1:c.8151A>T	ENSP00000505094.1:p.Ala2717=
ENST00000679882.1:c.12816A>T	ENSP00000506154.1:p.Ala4272=
ENST00000680029.1:c.3828A>T
ENST00000680877.1:c.8151A>T	ENSP00000505724.1:p.Ala2717=
ENST00000681923.1:n.2266A>T
ENST00000262189.10:c.13251A>T	ENSP00000262189.6:p.Ala4417=
ENST00000355193.6:c.13251A>T	ENSP00000347325.3:p.Ala4417=
ENST00000360104.7:c.5932A>T
ENST00000424877.5:c.3102A>T	ENSP00000410411.1:p.Ala1034=
ENST00000473186.5:n.11133A>T
ENST00000558084.5:c.*10771A>T	ENSP00000453752.1:n.*10771A>T
NM_170606.2:c.13251A>T	NP_733751.2:p.Ala4417=
XM_005250025.3:c.13467A>T	XP_005250082.1:p.Ala4489=
XM_005250026.2:c.13464A>T	XP_005250083.1:p.Ala4488=
XM_005250027.3:c.13464A>T	XP_005250084.1:p.Ala4488=
XM_005250028.3:c.13467A>T	XP_005250085.1:p.Ala4489=
XM_005250031.3:c.13302A>T	XP_005250088.1:p.Ala4434=
XM_006716077.2:c.13464A>T	XP_006716140.1:p.Ala4488=
XM_006716078.2:c.13395A>T	XP_006716141.1:p.Ala4465=
XM_006716079.2:c.13299A>T	XP_006716142.1:p.Ala4433=
XM_011516450.1:c.13419A>T	XP_011514752.1:p.Ala4473=
XM_011516451.1:c.13347A>T	XP_011514753.1:p.Ala4449=
XM_011516452.1:c.13314A>T	XP_011514754.1:p.Ala4438=
XM_011516453.1:c.13230A>T	XP_011514755.1:p.Ala4410=
XM_011516454.1:c.12552A>T	XP_011514756.1:p.Ala4184=
XM_011516455.1:c.11013A>T	XP_011514757.1:p.Ala3671=
XM_011516456.1:c.13419A>T	XP_011514758.1:p.Ala4473=
XM_005250025.4:c.13467A>T	XP_005250082.1:p.Ala4489=
XM_005250026.3:c.13464A>T	XP_005250083.1:p.Ala4488=
XM_005250027.4:c.13464A>T	XP_005250084.1:p.Ala4488=
XM_005250028.4:c.13467A>T	XP_005250085.1:p.Ala4489=
XM_005250031.4:c.13302A>T	XP_005250088.1:p.Ala4434=
XM_006716077.3:c.13464A>T	XP_006716140.1:p.Ala4488=
XM_006716078.3:c.13395A>T	XP_006716141.1:p.Ala4465=
XM_006716079.3:c.13299A>T	XP_006716142.1:p.Ala4433=
XM_011516450.2:c.13419A>T	XP_011514752.1:p.Ala4473=
XM_011516451.2:c.13347A>T	XP_011514753.1:p.Ala4449=
XM_011516452.2:c.13314A>T	XP_011514754.1:p.Ala4438=
XM_011516453.2:c.13230A>T	XP_011514755.1:p.Ala4410=
XM_011516454.2:c.12552A>T	XP_011514756.1:p.Ala4184=
XM_011516456.2:c.13419A>T	XP_011514758.1:p.Ala4473=
XM_017012480.1:c.13467A>T	XP_016867969.1:p.Ala4489=
XM_017012481.1:c.13464A>T	XP_016867970.1:p.Ala4488=
XM_017012482.1:c.13464A>T	XP_016867971.1:p.Ala4488=
XM_017012483.1:c.13464A>T	XP_016867972.1:p.Ala4488=
XM_017012484.1:c.13434A>T	XP_016867973.1:p.Ala4478=
XM_017012485.1:c.13416A>T	XP_016867974.1:p.Ala4472=
XM_017012486.1:c.13392A>T	XP_016867975.1:p.Ala4464=
XM_017012487.1:c.13320A>T	XP_016867976.1:p.Ala4440=
XM_017012488.1:c.13284A>T	XP_016867977.1:p.Ala4428=
XM_017012489.1:c.10137A>T	XP_016867978.1:p.Ala3379=
XM_017012490.2:c.9741A>T	XP_016867979.1:p.Ala3247=
XM_024446852.1:c.13464A>T	XP_024302620.1:p.Ala4488=
XM_024446853.1:c.13392A>T	XP_024302621.1:p.Ala4464=
NM_170606.3:c.13251A>T MANE Select	NP_733751.2:p.Ala4417=