Canonical Allele Identifier: CA1980500775

Gene: KMT5B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68158253_68158256delinsCTCT , CM000673.2:g.68158253_68158256delinsCTCT	GRCh38
NC_000011.9:g.67925720_67925723delinsCTCT , CM000673.1:g.67925720_67925723delinsCTCT	GRCh37
NC_000011.8:g.67682296_67682299delinsCTCT	NCBI36
NG_052873.1:g.60517_60520delinsAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453170.6:c.1877_1880delinsAGAG	ENSP00000406377.2:p.Lys626=
ENST00000524672.3:n.2442_2445delinsAGAG
ENST00000700520.1:c.*1714_*1717delinsAGAG	ENSP00000515027.1:n.*1714_*1717delinsAGAG
ENST00000700521.1:c.*1757_*1760delinsAGAG	ENSP00000515028.1:n.*1757_*1760delinsAGAG
ENST00000700522.1:c.*1757_*1760delinsAGAG	ENSP00000515029.1:n.*1757_*1760delinsAGAG
ENST00000700523.1:c.1574_1577delinsAGAG	ENSP00000515030.1:p.Lys525=
ENST00000700524.1:c.*1298_*1301delinsAGAG	ENSP00000515031.1:n.*1298_*1301delinsAGAG
ENST00000304363.9:c.2090_2093delinsAGAG MANE Select	ENSP00000305899.4:p.Lys697=
ENST00000304363.8:c.2090_2093delinsAGAG	ENSP00000305899.4:p.Lys697=
ENST00000441488.6:c.*1298_*1301delinsAGAG	ENSP00000411146.2:n.*1298_*1301delinsAGAG
ENST00000615954.4:c.2090_2093delinsAGAG	ENSP00000484858.1:p.Lys697=
NM_001300907.1:c.1574_1577delinsAGAG	NP_001287836.1:p.Lys525=
NM_001300908.1:c.1370_1373delinsAGAG	NP_001287837.1:p.Lys457=
NM_017635.4:c.2090_2093delinsAGAG	NP_060105.3:p.Lys697=
XM_005274035.2:c.2090_2093delinsAGAG	XP_005274092.2:p.Lys697=
XM_005274036.2:c.2021_2024delinsAGAG	XP_005274093.2:p.Lys674=
XM_005274037.1:c.1574_1577delinsAGAG	XP_005274094.1:p.Lys525=
XM_006718581.1:c.2021_2024delinsAGAG	XP_006718644.1:p.Lys674=
XM_011545091.1:c.2090_2093delinsAGAG	XP_011543393.1:p.Lys697=
XM_011545092.1:c.1877_1880delinsAGAG	XP_011543394.1:p.Lys626=
XM_011545093.1:c.848_851delinsAGAG	XP_011543395.1:p.Lys283=
XM_005274035.4:c.2090_2093delinsAGAG	XP_005274092.2:p.Lys697=
XM_005274036.4:c.2021_2024delinsAGAG	XP_005274093.2:p.Lys674=
XM_006718581.2:c.2021_2024delinsAGAG	XP_006718644.1:p.Lys674=
XM_011545092.3:c.1877_1880delinsAGAG	XP_011543394.1:p.Lys626=
XM_017017876.2:c.1574_1577delinsAGAG	XP_016873365.1:p.Lys525=
XM_017017877.2:c.1574_1577delinsAGAG	XP_016873366.1:p.Lys525=
XM_017017878.2:c.1574_1577delinsAGAG	XP_016873367.1:p.Lys525=
XM_017017879.2:c.1574_1577delinsAGAG	XP_016873368.1:p.Lys525=
XM_024448570.1:c.848_851delinsAGAG	XP_024304338.1:p.Lys283=
NM_017635.5:c.2090_2093delinsAGAG MANE Select	NP_060105.3:p.Lys697=
NM_001300908.2:c.1370_1373delinsAGAG	NP_001287837.1:p.Lys457=
NM_001369426.1:c.2090_2093delinsAGAG	NP_001356355.1:p.Lys697=
NM_001369428.1:c.1574_1577delinsAGAG	NP_001356357.1:p.Lys525=
NM_001369429.1:c.1574_1577delinsAGAG	NP_001356358.1:p.Lys525=
NM_001369430.1:c.1574_1577delinsAGAG	NP_001356359.1:p.Lys525=
NM_001369431.1:c.1574_1577delinsAGAG	NP_001356360.1:p.Lys525=
NM_001369432.1:c.1574_1577delinsAGAG	NP_001356361.1:p.Lys525=
NM_001369433.1:c.1574_1577delinsAGAG	NP_001356362.1:p.Lys525=