Canonical Allele Identifier: CA600238789

Gene: KMT5B

Linked Data

• dbSNP Id: rs1408911204
• gnomAD v2: 11-67925316-CAGA-C
• gnomAD v4: 11-68157849-CAGA-C
• MyVariant Identifiers: chr11:g.67925317_67925319del (hg19) ; chr11:g.68157850_68157852del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68157853_68157855del , CM000673.2:g.68157853_68157855del	GRCh38
NC_000011.9:g.67925320_67925322del , CM000673.1:g.67925320_67925322del	GRCh37
NC_000011.8:g.67681896_67681898del	NCBI36
NG_052873.1:g.60921_60923del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453170.6:c.2281_2283del	ENSP00000406377.2:p.Ser761del
ENST00000524672.3:n.2846_2848del
ENST00000700520.1:c.*2118_*2120del	ENSP00000515027.1:n.*2118_*2120del
ENST00000700521.1:c.*2161_*2163del	ENSP00000515028.1:n.*2161_*2163del
ENST00000700522.1:c.*2161_*2163del	ENSP00000515029.1:n.*2161_*2163del
ENST00000700523.1:c.1978_1980del	ENSP00000515030.1:p.Ser660del
ENST00000700524.1:c.*1702_*1704del	ENSP00000515031.1:n.*1702_*1704del
ENST00000304363.9:c.2494_2496del MANE Select	ENSP00000305899.4:p.Ser832del
ENST00000304363.8:c.2494_2496del	ENSP00000305899.4:p.Ser832del
ENST00000441488.6:c.*1702_*1704del	ENSP00000411146.2:n.*1702_*1704del
ENST00000615954.4:c.2494_2496del	ENSP00000484858.1:p.Ser832del
NM_001300907.1:c.1978_1980del	NP_001287836.1:p.Ser660del
NM_001300908.1:c.1774_1776del	NP_001287837.1:p.Ser592del
NM_017635.4:c.2494_2496del	NP_060105.3:p.Ser832del
XM_005274035.2:c.2494_2496del	XP_005274092.2:p.Ser832del
XM_005274036.2:c.2425_2427del	XP_005274093.2:p.Ser809del
XM_005274037.1:c.1978_1980del	XP_005274094.1:p.Ser660del
XM_006718581.1:c.2425_2427del	XP_006718644.1:p.Ser809del
XM_011545091.1:c.2494_2496del	XP_011543393.1:p.Ser832del
XM_011545092.1:c.2281_2283del	XP_011543394.1:p.Ser761del
XM_011545093.1:c.1252_1254del	XP_011543395.1:p.Ser418del
XM_005274035.4:c.2494_2496del	XP_005274092.2:p.Ser832del
XM_005274036.4:c.2425_2427del	XP_005274093.2:p.Ser809del
XM_006718581.2:c.2425_2427del	XP_006718644.1:p.Ser809del
XM_011545092.3:c.2281_2283del	XP_011543394.1:p.Ser761del
XM_017017876.2:c.1978_1980del	XP_016873365.1:p.Ser660del
XM_017017877.2:c.1978_1980del	XP_016873366.1:p.Ser660del
XM_017017878.2:c.1978_1980del	XP_016873367.1:p.Ser660del
XM_017017879.2:c.1978_1980del	XP_016873368.1:p.Ser660del
XM_024448570.1:c.1252_1254del	XP_024304338.1:p.Ser418del
NM_017635.5:c.2494_2496del MANE Select	NP_060105.3:p.Ser832del
NM_001300908.2:c.1774_1776del	NP_001287837.1:p.Ser592del
NM_001369426.1:c.2494_2496del	NP_001356355.1:p.Ser832del
NM_001369428.1:c.1978_1980del	NP_001356357.1:p.Ser660del
NM_001369429.1:c.1978_1980del	NP_001356358.1:p.Ser660del
NM_001369430.1:c.1978_1980del	NP_001356359.1:p.Ser660del
NM_001369431.1:c.1978_1980del	NP_001356360.1:p.Ser660del
NM_001369432.1:c.1978_1980del	NP_001356361.1:p.Ser660del
NM_001369433.1:c.1978_1980del	NP_001356362.1:p.Ser660del