Canonical Allele Identifier: CA387004695

Gene: SETD1B

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121827749G>C , CM000674.2:g.121827749G>C	GRCh38
NC_000012.11:g.122265655G>C , CM000674.1:g.122265655G>C	GRCh37
NC_000012.10:g.120750038G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000604567.6:c.5484G>C MANE Select	ENSP00000474253.1:p.Lys1828Asn
ENST00000267197.9:c.5355G>C	ENSP00000267197.6:p.Lys1785Asn
ENST00000542440.5:c.5355G>C	ENSP00000442924.1:p.Lys1785Asn
ENST00000604567.5:c.5484G>C	ENSP00000474253.1:p.Lys1828Asn
ENST00000619791.1:c.5484G>C	ENSP00000481531.1:p.Lys1828Asn
NM_015048.1:c.5355G>C	NP_055863.1:p.Lys1785Asn
XM_005253858.3:c.5484G>C	XP_005253915.1:p.Lys1828Asn
XM_006719296.2:c.5484G>C	XP_006719359.1:p.Lys1828Asn
XM_011538053.1:c.5484G>C	XP_011536355.1:p.Lys1828Asn
NM_001353345.1:c.5484G>C	NP_001340274.1:p.Lys1828Asn
XM_005253858.4:c.5484G>C	XP_005253915.1:p.Lys1828Asn
XM_006719296.3:c.5484G>C	XP_006719359.1:p.Lys1828Asn
XM_024448898.1:c.5484G>C	XP_024304666.1:p.Lys1828Asn
NM_001353345.2:c.5484G>C MANE Select	NP_001340274.1:p.Lys1828Asn