Canonical Allele Identifier: CA458884848

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845926A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148841A>T , CM000669.2:g.152148841A>T	GRCh38
NC_000007.13:g.151845926A>T , CM000669.1:g.151845926A>T	GRCh37
NC_000007.12:g.151476859A>T	NCBI36
NG_033948.1:g.292165T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1274T>A
ENST00000682116.1:n.2218T>A
ENST00000682283.1:c.13257T>A	ENSP00000507485.1:p.Ile4419=
ENST00000682629.1:n.2386T>A
ENST00000683120.1:n.8278T>A
ENST00000683178.1:c.3659T>A
ENST00000683200.1:c.10596T>A	ENSP00000508052.1:p.Ile3532=
ENST00000683337.1:n.4716T>A
ENST00000683502.1:c.3731T>A
ENST00000683621.1:n.1852T>A
ENST00000683640.1:n.1802T>A
ENST00000684069.1:c.1503T>A	ENSP00000507650.1:p.Ile501=
ENST00000684261.1:c.7983T>A	ENSP00000508097.1:p.Ile2661=
ENST00000684649.1:c.3731T>A
ENST00000262189.11:c.13086T>A MANE Select	ENSP00000262189.6:p.Ile4362=
ENST00000360104.8:c.8873T>A
ENST00000418061.2:c.3728T>A
ENST00000424877.6:c.3662T>A
ENST00000679393.1:n.7797T>A
ENST00000679560.1:c.7986T>A	ENSP00000505094.1:p.Ile2662=
ENST00000679882.1:c.12651T>A	ENSP00000506154.1:p.Ile4217=
ENST00000680029.1:c.3663T>A
ENST00000680877.1:c.7986T>A	ENSP00000505724.1:p.Ile2662=
ENST00000681923.1:n.2101T>A
ENST00000262189.10:c.13086T>A	ENSP00000262189.6:p.Ile4362=
ENST00000355193.6:c.13086T>A	ENSP00000347325.3:p.Ile4362=
ENST00000360104.7:c.5767T>A
ENST00000424877.5:c.2937T>A	ENSP00000410411.1:p.Ile979=
ENST00000473186.5:n.10968T>A
ENST00000558084.5:c.*10606T>A	ENSP00000453752.1:n.*10606T>A
NM_170606.2:c.13086T>A	NP_733751.2:p.Ile4362=
XM_005250025.3:c.13302T>A	XP_005250082.1:p.Ile4434=
XM_005250026.2:c.13299T>A	XP_005250083.1:p.Ile4433=
XM_005250027.3:c.13299T>A	XP_005250084.1:p.Ile4433=
XM_005250028.3:c.13302T>A	XP_005250085.1:p.Ile4434=
XM_005250031.3:c.13137T>A	XP_005250088.1:p.Ile4379=
XM_006716077.2:c.13299T>A	XP_006716140.1:p.Ile4433=
XM_006716078.2:c.13230T>A	XP_006716141.1:p.Ile4410=
XM_006716079.2:c.13134T>A	XP_006716142.1:p.Ile4378=
XM_011516450.1:c.13254T>A	XP_011514752.1:p.Ile4418=
XM_011516451.1:c.13182T>A	XP_011514753.1:p.Ile4394=
XM_011516452.1:c.13149T>A	XP_011514754.1:p.Ile4383=
XM_011516453.1:c.13065T>A	XP_011514755.1:p.Ile4355=
XM_011516454.1:c.12387T>A	XP_011514756.1:p.Ile4129=
XM_011516455.1:c.10848T>A	XP_011514757.1:p.Ile3616=
XM_011516456.1:c.13254T>A	XP_011514758.1:p.Ile4418=
XM_005250025.4:c.13302T>A	XP_005250082.1:p.Ile4434=
XM_005250026.3:c.13299T>A	XP_005250083.1:p.Ile4433=
XM_005250027.4:c.13299T>A	XP_005250084.1:p.Ile4433=
XM_005250028.4:c.13302T>A	XP_005250085.1:p.Ile4434=
XM_005250031.4:c.13137T>A	XP_005250088.1:p.Ile4379=
XM_006716077.3:c.13299T>A	XP_006716140.1:p.Ile4433=
XM_006716078.3:c.13230T>A	XP_006716141.1:p.Ile4410=
XM_006716079.3:c.13134T>A	XP_006716142.1:p.Ile4378=
XM_011516450.2:c.13254T>A	XP_011514752.1:p.Ile4418=
XM_011516451.2:c.13182T>A	XP_011514753.1:p.Ile4394=
XM_011516452.2:c.13149T>A	XP_011514754.1:p.Ile4383=
XM_011516453.2:c.13065T>A	XP_011514755.1:p.Ile4355=
XM_011516454.2:c.12387T>A	XP_011514756.1:p.Ile4129=
XM_011516456.2:c.13254T>A	XP_011514758.1:p.Ile4418=
XM_017012480.1:c.13302T>A	XP_016867969.1:p.Ile4434=
XM_017012481.1:c.13299T>A	XP_016867970.1:p.Ile4433=
XM_017012482.1:c.13299T>A	XP_016867971.1:p.Ile4433=
XM_017012483.1:c.13299T>A	XP_016867972.1:p.Ile4433=
XM_017012484.1:c.13269T>A	XP_016867973.1:p.Ile4423=
XM_017012485.1:c.13251T>A	XP_016867974.1:p.Ile4417=
XM_017012486.1:c.13227T>A	XP_016867975.1:p.Ile4409=
XM_017012487.1:c.13155T>A	XP_016867976.1:p.Ile4385=
XM_017012488.1:c.13119T>A	XP_016867977.1:p.Ile4373=
XM_017012489.1:c.9972T>A	XP_016867978.1:p.Ile3324=
XM_017012490.2:c.9576T>A	XP_016867979.1:p.Ile3192=
XM_024446852.1:c.13299T>A	XP_024302620.1:p.Ile4433=
XM_024446853.1:c.13227T>A	XP_024302621.1:p.Ile4409=
NM_170606.3:c.13086T>A MANE Select	NP_733751.2:p.Ile4362=