Canonical Allele Identifier: CA381588634

Gene: KMT5B

Linked Data

• dbSNP Id: rs1474640095
• gnomAD v2: 11-67925642-T-C
• gnomAD v4: 11-68158175-T-C
• MyVariant Identifiers: chr11:g.67925642T>C (hg19) ; chr11:g.68158175T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68158175T>C , CM000673.2:g.68158175T>C	GRCh38
NC_000011.9:g.67925642T>C , CM000673.1:g.67925642T>C	GRCh37
NC_000011.8:g.67682218T>C	NCBI36
NG_052873.1:g.60598A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453170.6:c.1958A>G	ENSP00000406377.2:p.His653Arg
ENST00000524672.3:n.2523A>G
ENST00000700520.1:c.*1795A>G	ENSP00000515027.1:n.*1795A>G
ENST00000700521.1:c.*1838A>G	ENSP00000515028.1:n.*1838A>G
ENST00000700522.1:c.*1838A>G	ENSP00000515029.1:n.*1838A>G
ENST00000700523.1:c.1655A>G	ENSP00000515030.1:p.His552Arg
ENST00000700524.1:c.*1379A>G	ENSP00000515031.1:n.*1379A>G
ENST00000304363.9:c.2171A>G MANE Select	ENSP00000305899.4:p.His724Arg
ENST00000304363.8:c.2171A>G	ENSP00000305899.4:p.His724Arg
ENST00000441488.6:c.*1379A>G	ENSP00000411146.2:n.*1379A>G
ENST00000615954.4:c.2171A>G	ENSP00000484858.1:p.His724Arg
NM_001300907.1:c.1655A>G	NP_001287836.1:p.His552Arg
NM_001300908.1:c.1451A>G	NP_001287837.1:p.His484Arg
NM_017635.4:c.2171A>G	NP_060105.3:p.His724Arg
XM_005274035.2:c.2171A>G	XP_005274092.2:p.His724Arg
XM_005274036.2:c.2102A>G	XP_005274093.2:p.His701Arg
XM_005274037.1:c.1655A>G	XP_005274094.1:p.His552Arg
XM_006718581.1:c.2102A>G	XP_006718644.1:p.His701Arg
XM_011545091.1:c.2171A>G	XP_011543393.1:p.His724Arg
XM_011545092.1:c.1958A>G	XP_011543394.1:p.His653Arg
XM_011545093.1:c.929A>G	XP_011543395.1:p.His310Arg
XM_005274035.4:c.2171A>G	XP_005274092.2:p.His724Arg
XM_005274036.4:c.2102A>G	XP_005274093.2:p.His701Arg
XM_006718581.2:c.2102A>G	XP_006718644.1:p.His701Arg
XM_011545092.3:c.1958A>G	XP_011543394.1:p.His653Arg
XM_017017876.2:c.1655A>G	XP_016873365.1:p.His552Arg
XM_017017877.2:c.1655A>G	XP_016873366.1:p.His552Arg
XM_017017878.2:c.1655A>G	XP_016873367.1:p.His552Arg
XM_017017879.2:c.1655A>G	XP_016873368.1:p.His552Arg
XM_024448570.1:c.929A>G	XP_024304338.1:p.His310Arg
NM_017635.5:c.2171A>G MANE Select	NP_060105.3:p.His724Arg
NM_001300908.2:c.1451A>G	NP_001287837.1:p.His484Arg
NM_001369426.1:c.2171A>G	NP_001356355.1:p.His724Arg
NM_001369428.1:c.1655A>G	NP_001356357.1:p.His552Arg
NM_001369429.1:c.1655A>G	NP_001356358.1:p.His552Arg
NM_001369430.1:c.1655A>G	NP_001356359.1:p.His552Arg
NM_001369431.1:c.1655A>G	NP_001356360.1:p.His552Arg
NM_001369432.1:c.1655A>G	NP_001356361.1:p.His552Arg
NM_001369433.1:c.1655A>G	NP_001356362.1:p.His552Arg