Canonical Allele Identifier: CA2133508304

Gene: KLHL28

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.44934496C= , CM000676.2:g.44934496C=	GRCh38
NC_000014.8:g.45403699C= , CM000676.1:g.45403699C=	GRCh37
NC_000014.7:g.44473449C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017658.5:c.962G= MANE Select	NP_060128.2:p.Arg321=
ENST00000396128.9:c.962G= MANE Select	ENSP00000379434.4:p.Arg321=
NM_001308112.1:c.1004G=	NP_001295041.1:p.Arg335=
NM_001308112.2:c.1004G=	NP_001295041.1:p.Arg335=
NM_017658.3:c.962G=	NP_060128.2:p.Arg321=
NM_017658.4:c.962G=	NP_060128.2:p.Arg321=
ENST00000355081.3:c.1004G=	ENSP00000347193.2:p.Arg335=
ENST00000396128.8:c.962G=	ENSP00000379434.3:p.Arg321=
XM_005267770.2:c.962G=	XP_005267827.1:p.Arg321=
XM_005267770.4:c.962G=	XP_005267827.1:p.Arg321=
XM_011536847.1:c.962G=	XP_011535149.1:p.Arg321=
XM_011536847.3:c.962G=	XP_011535149.1:p.Arg321=
XM_011536848.1:c.962G=	XP_011535150.1:p.Arg321=
XM_011536849.1:c.1004G=	XP_011535151.1:p.Arg335=
XM_011536849.2:c.1004G=	XP_011535151.1:p.Arg335=
XM_024449635.1:c.962G=	XP_024305403.1:p.Arg321=