Canonical Allele Identifier: CA370091457

Gene: KMT2C

Linked Data

• MyVariant Identifiers: chr7:g.151845665A>T (hg19) ; chr7:g.152148580A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152148580A>T , CM000669.2:g.152148580A>T	GRCh38
NC_000007.13:g.151845665A>T , CM000669.1:g.151845665A>T	GRCh37
NC_000007.12:g.151476598A>T	NCBI36
NG_033948.1:g.292426T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682040.1:c.1535T>A
ENST00000682116.1:n.2479T>A
ENST00000682283.1:c.13518T>A	ENSP00000507485.1:p.Asn4506Lys
ENST00000682629.1:n.2647T>A
ENST00000683120.1:n.8539T>A
ENST00000683178.1:c.3920T>A
ENST00000683200.1:c.10857T>A	ENSP00000508052.1:p.Asn3619Lys
ENST00000683337.1:n.4977T>A
ENST00000683502.1:c.3992T>A
ENST00000683621.1:n.2113T>A
ENST00000683640.1:n.2063T>A
ENST00000684069.1:c.1764T>A	ENSP00000507650.1:p.Asn588Lys
ENST00000684261.1:c.8244T>A	ENSP00000508097.1:p.Asn2748Lys
ENST00000684391.1:n.105T>A
ENST00000684649.1:c.3992T>A
ENST00000262189.11:c.13347T>A MANE Select	ENSP00000262189.6:p.Asn4449Lys
ENST00000360104.8:c.9134T>A
ENST00000418061.2:c.3989T>A
ENST00000424877.6:c.3923T>A
ENST00000679393.1:n.8058T>A
ENST00000679560.1:c.8247T>A	ENSP00000505094.1:p.Asn2749Lys
ENST00000679882.1:c.12912T>A	ENSP00000506154.1:p.Asn4304Lys
ENST00000680029.1:c.3924T>A
ENST00000680877.1:c.8247T>A	ENSP00000505724.1:p.Asn2749Lys
ENST00000681923.1:n.2362T>A
ENST00000262189.10:c.13347T>A	ENSP00000262189.6:p.Asn4449Lys
ENST00000355193.6:c.13347T>A	ENSP00000347325.3:p.Asn4449Lys
ENST00000360104.7:c.6028T>A
ENST00000424877.5:c.3198T>A	ENSP00000410411.1:p.Asn1066Lys
ENST00000473186.5:n.11229T>A
ENST00000558084.5:c.*10867T>A	ENSP00000453752.1:n.*10867T>A
NM_170606.2:c.13347T>A	NP_733751.2:p.Asn4449Lys
XM_005250025.3:c.13563T>A	XP_005250082.1:p.Asn4521Lys
XM_005250026.2:c.13560T>A	XP_005250083.1:p.Asn4520Lys
XM_005250027.3:c.13560T>A	XP_005250084.1:p.Asn4520Lys
XM_005250028.3:c.13563T>A	XP_005250085.1:p.Asn4521Lys
XM_005250031.3:c.13398T>A	XP_005250088.1:p.Asn4466Lys
XM_006716077.2:c.13560T>A	XP_006716140.1:p.Asn4520Lys
XM_006716078.2:c.13491T>A	XP_006716141.1:p.Asn4497Lys
XM_006716079.2:c.13395T>A	XP_006716142.1:p.Asn4465Lys
XM_011516450.1:c.13515T>A	XP_011514752.1:p.Asn4505Lys
XM_011516451.1:c.13443T>A	XP_011514753.1:p.Asn4481Lys
XM_011516452.1:c.13410T>A	XP_011514754.1:p.Asn4470Lys
XM_011516453.1:c.13326T>A	XP_011514755.1:p.Asn4442Lys
XM_011516454.1:c.12648T>A	XP_011514756.1:p.Asn4216Lys
XM_011516455.1:c.11109T>A	XP_011514757.1:p.Asn3703Lys
XM_011516456.1:c.13515T>A	XP_011514758.1:p.Asn4505Lys
XM_005250025.4:c.13563T>A	XP_005250082.1:p.Asn4521Lys
XM_005250026.3:c.13560T>A	XP_005250083.1:p.Asn4520Lys
XM_005250027.4:c.13560T>A	XP_005250084.1:p.Asn4520Lys
XM_005250028.4:c.13563T>A	XP_005250085.1:p.Asn4521Lys
XM_005250031.4:c.13398T>A	XP_005250088.1:p.Asn4466Lys
XM_006716077.3:c.13560T>A	XP_006716140.1:p.Asn4520Lys
XM_006716078.3:c.13491T>A	XP_006716141.1:p.Asn4497Lys
XM_006716079.3:c.13395T>A	XP_006716142.1:p.Asn4465Lys
XM_011516450.2:c.13515T>A	XP_011514752.1:p.Asn4505Lys
XM_011516451.2:c.13443T>A	XP_011514753.1:p.Asn4481Lys
XM_011516452.2:c.13410T>A	XP_011514754.1:p.Asn4470Lys
XM_011516453.2:c.13326T>A	XP_011514755.1:p.Asn4442Lys
XM_011516454.2:c.12648T>A	XP_011514756.1:p.Asn4216Lys
XM_011516456.2:c.13515T>A	XP_011514758.1:p.Asn4505Lys
XM_017012480.1:c.13563T>A	XP_016867969.1:p.Asn4521Lys
XM_017012481.1:c.13560T>A	XP_016867970.1:p.Asn4520Lys
XM_017012482.1:c.13560T>A	XP_016867971.1:p.Asn4520Lys
XM_017012483.1:c.13560T>A	XP_016867972.1:p.Asn4520Lys
XM_017012484.1:c.13530T>A	XP_016867973.1:p.Asn4510Lys
XM_017012485.1:c.13512T>A	XP_016867974.1:p.Asn4504Lys
XM_017012486.1:c.13488T>A	XP_016867975.1:p.Asn4496Lys
XM_017012487.1:c.13416T>A	XP_016867976.1:p.Asn4472Lys
XM_017012488.1:c.13380T>A	XP_016867977.1:p.Asn4460Lys
XM_017012489.1:c.10233T>A	XP_016867978.1:p.Asn3411Lys
XM_017012490.2:c.9837T>A	XP_016867979.1:p.Asn3279Lys
XM_024446852.1:c.13560T>A	XP_024302620.1:p.Asn4520Lys
XM_024446853.1:c.13488T>A	XP_024302621.1:p.Asn4496Lys
NM_170606.3:c.13347T>A MANE Select	NP_733751.2:p.Asn4449Lys